Compositions for Inhibiting Gene Expression and Uses Thereof

ABSTRACT

The inventors have examined the means for providing more efficacious miRNA blocking compounds. The inventors have discovered new structural features that surprisingly improve the efficacy of miRNA blocking molecules. These features include the presence of multiple 3′ ends and a linker at the 5′ ends. Surprisingly, these features improve the efficacy of the gene expression blocking compounds in a manner that decreases the compound&#39;s biologic instability. Even more surprisingly, this effect has been found to be applicable to both DNA and RNA oligonucleotide-based compounds and to have application in traditional antisense and RNAi technology.

RELATED APPLICATIONS

This application is a continuation application of U.S. patent application Ser. No. 13/072,017, filed on Mar. 25, 2011, the contents of which is incorporated herein by reference in its entirety.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to compounds, compositions, and methods of use for the inhibition of gene expression and/or activity or for diagnosing, treating and/or preventing diseases and/or conditions that respond to the inhibition of gene expression and/or activity.

2. Summary of the Related Art

An approach to inhibit gene expression is antisense technology or RNA inhibition (RNAi). These approaches make use of sequence-specific binding of DNA and/or RNA based oligonucleotides to selected mRNA, microRNA, preRNA or mitochondrial RNA targets and the inhibition of translation that results therefrom. This oligonucleotide-based inhibition of translation and ultimately gene expression is the result of one or more cellular mechanisms, which may include but is not limited to (i) direct (steric) blockage of translation, (ii) RNase H-mediated inhibition, and (iii) RNAi-mediated inhibition (e.g. short interfering-RNA (siRNA), microRNA (miRNA), DNA-directed-RNAi (ddRNAi), and single-stranded RNAi (ssRNAi)).

The history of antisense technology has revealed that while determination of antisense oligonucleotides that bind to mRNA is relatively straight forward, the optimization of antisense oligonucleotides that have true potential to inhibit gene expression and therefore be good clinical candidates is not. Accordingly, if an oligonucleotide-based approach to down-regulating gene expression is to be successful, there is a need for optimized antisense oligonucleotides that most efficiently achieve this result. Such optimized antisense oligonucleotides could be used alone or in conjunction with other prophylactic and/or therapeutic compositions.

Since Zamecnik & Stephenson published the first demonstration of using antisense oligonucleotides as a means to inhibit translation of viral proteins (Zemecnik and Stephenson (1978) Proc. Natl. Acad. Sci. 75: 285-288), there has been great interest in utilizing oligonucleotide-based compounds to inhibit expression of genes. These initial efforts utilized single-stranded, unmodified oligodeoxyribonucleotides or oligoribonucleotides (Agrawal et al. (1992) Ann. NY Acad. Sci. 660:2-10), which are inherently unstable in vivo, to bind to mRNA in vivo and create a double-stranded RNA template for enzymatic, or RNAse, degradation. Subsequent efforts were made to determine the utility of oligodeoxyribonucleotides that incorporated nuclease-resistant phosphorothioate and/or methylphosphonate linkages (Agrawal et. al (1988) Proc. Natl. Acad. Sci. 85:7079-7083; Metelev & Agrawal U.S. Pat. No. 5,652,355; Metelev & Agrawal U.S. Pat. No. 6,143,881; Matsukura et al. (1987) Proc. Natl. Acad. Sci. 84:7706).

Another class of RNA-based molecules that inhibit gene expression are referred to as ribozymes. Ribozymes form stem loop structures and bind to an RNA target to mediate its cleavage directly (Cech, T. (1990) Ann. Rev. Biochem. 59:543). Ribozymes selectively bind to target-RNA and catalyze a transesterification or a hydrolysis reaction to cleave specific phosphodiester linkages in single-stranded RNA. If introduced into cells, ribozymes have the potential to bind to target-mRNA and inhibit translation of such mRNA. As with single-stranded antisense technologies, the stability and activity of ribozymes have been improved through incorporation of certain chemical modifications into the ribozyme structure (Goodchild U.S. Pat. No. 6,204,027; Goodchild U.S. Pat. No. 6,573,072). While antisense oligonucleotide and ribozyme technologies continue to advance, discoveries with other oligonucleotide-based technologies are being made.

Based on the pioneering discoveries of Fire and Mello (Fire et al. (1998) Nature, 391:806-811), efforts have turned toward RNA-interfering (RNAi) technologies (e.g. short interfering-RNA (siRNA), microRNA (miRNA), DNA-directed-RNAi (ddRNAi), and single-stranded RNAi (ssRNAi)) in mammalian systems. RNAi refers to the process of post-transcriptional inhibition of gene expression using short oligonucleotides that are designed to hybridize to specific mRNA targets (Fire et al. (1998) Nature 391:806-811; Zamore et al. (2000) Cell, 101:25-33). In the case of siRNA, short, double-stranded RNA molecules utilize cellular enzymatic machinery to cleave homologous target RNA molecules. (Rana (2007) Nature Rev. Mol. Cell. Biol. 8:23-36). Double-stranded RNAi technologies rely upon administration or expression of double stranded RNA (dsRNA), which once inside the cell, is bound by an enzyme called dicer and cleaved into 21-23 nucleotides. The resulting dicer-dsRNA complex is delivered to and interacts with an Argonaut-containing complex of proteins referred to as an RNA-induced silencing complex (RISC). RISC is thought to be present in cells to catalytically break down specific mRNA molecules. Once bound by RISC, the dsRNA is unwound resulting in a ssRNA-RISC complex, which is able to hybridize to targeted mRNA. Once hybridized, the RISC complex breaks down the mRNA. In some cases, the dsRNA specific processes of dicer have been circumvented using single-stranded RNAi (ssRNAi) compositions that interact directly with RISC to achieve inhibition of gene expression (Holen et al. (2003) Nuc. Acids Res. 31:2401-2407). Although RNAi technologies are able to selectively bind to target mRNA, such molecules have also been recognized to induce non-specific immune stimulation through interaction with TLR3 (Kleinman et al., (2008) Nature 452:591-597; De Veer et. al. (2005) Immun. Cell Bio. 83:224-228; Kariko et al. (2004) J. Immunol. 172:6545-6549). This non-specific immune activation has raised questions as to the utility of RNAi technologies as pharmaceutical agents.

In the case of miRNA, a pri-miRNA is encoded in the genome of animals and plants. The pri-miRNA is a short, double stranded ribonucleic acid molecule that contains a hairpin loop. The pri-miRNA is transcribed in the nucleus and processed by the enzyme Drosha to create a double stranded, RNA molecule with a two-nucleotide overhang on its 3′ end. Once processed by Drosha, the pri-miRNA is exported into the cell's cytoplasm by a process involving Exportin-5. In the cytoplasm, the pri-miRNA is cleaved by the enzyme Dicer into shorter, double stranded segments of between 18 and 23 nucleotides, which retain the two-nucleotide overhang on the 3′ end. The resulting molecule is a mature miRNA that has antisense and sense sequences. Dicer unwinds the double stranded miRNA and one of the strands of the miRNA is incorporated into RISC, which facilitates the interaction of the miRNA with its target. The miRNA can function to regulate the expression of multiple genes by binding to the 3′-untranslated regions of specific mRNAs. In the case of plants, the miRNA may bind to a target site located within the 3′-untranslated region or within the coding region. Once bound to the target mRNA, the miRNA induces gene silencing by either mRNA degradation or inhibiting the mRNA from being translated. If the sequence is identical to the target, then the mRNA is degraded. If the sequence contains mismatched basepairs from the target, then the mRNA is inhibited from being translated. miRNAs are highly conserved and thought to be a vital component to regulating gene expression.

Although each of the antisense-based technologies has been used with some success, as a result of being based on oligonucleotides, each of these technologies has the inherent problem of being unstable in vivo and having the potential to produce off-target effects, for example unintended immune stimulation (Agrawal & Kandimalla (2004) Nature Biotech. 22:1533-1537). In the case of dsRNA, these oligonucleotides appear to have the additional issue of inefficient, in vivo delivery to cells (Medarova et. al (2007) Nature Med. 13:372-377). Despite many clinical trials of antisense oligonucleotide drug candidates, only one such compound has been approved as a drug by the FDA. This antisense compound was approved for treating CMV, but has never been marketed as a product. Additionally, no ribozyme or siRNA drug candidate has yet been approved by the FDA.

Approaches to optimizing each of these technologies have focused on addressing biostability, target recognition (e.g., cell permeability, thermostability), and in vivo activity. Often, these have represented competing considerations. For example, traditional antisense oligonucleotides utilized phosphate ester internucleotide linkages, which proved to be too biologically unstable to be effective. Thus, there was a focus on modifying antisense oligonucleotides to render them more biologically stable. Early approaches focused on modifying the internucleotide linkages to make them more resistant to degradation by cellular nucleases. These approaches led to the development of antisense oligonucleotides having a variety of non-naturally occurring internucleotide linkages, such as phosphorothioate, methylphosphonate (Sarin et al. (1988) Proc. Natl. Acad. Sci. 85:7448-7451), and peptide based linkages. (Matsukura et. al (1987) Proc. Natl. Acad. Sci. 84:7706; Agrawal et al. (1988) Proc. Natl. Acad. Sci. 85:7079-7083; Miller (1991) Bio-Technology 9:358). However, these modifications caused the molecules to decrease their target specificity and produced unwanted biological activities.

Later approaches to improve stability and retain specificity and biologic activity utilized mixed backbone oligonucleotides, which contain phosphodiester and phosphorothioate internucleotide linkages. This mixed backbone resulted in oligonucleotides that retained or improved their biological stability as compared to oligonucleotides with only phosphodiester linkages (Agrawal et al. (1990) Proc. Natl. Acad. Sci. 87:1401-1405; US Patent Publication No. 20010049436). Throughout oligonucleotide research, it has been recognized that these molecules are succeptable in vivo to degradation by exonucleases, with the primary degradation occurring from the 3′-end of the molecule (Shaw et. al (1991) Nucleic Acids Res. 19:747-750; Temsamani et al. (1993) Analytical Bioc. 215:54-58). As such, approaches to avoid this exonuclease activity have utilized (i) capping structures at the 5′ and/or 3′ termini (Tesamani et. al (1992) Ann. NY Acad. Sci. 660:318-320; Temsamani et al. (1993) Antisense Res. Dev. 3:277-284; Tang et al. (1993) Nucl. Acids Res. 20:2729-2735), (ii) linking two or more oligonucleotides through 5′-3′,5′-2,2′-3′,3′-2′ or 3′-3′ linkages between the molecules (Agrawal et al. U.S. Pat. No. 6,489,464), (iii) self-hybridizing oligonucleotides that fold back on themselves at the 3′-end, which creates a hair-pin and removes the point of access for 3′-exonuclease activity to begin (Tang et al. (1993) Nucl. Acids Res. 20:2729-2735), or (iv) incorporating RNA into the oligonucleotide molecule, thus creating an RNA/DNA hybrid molecule (Metelev at al. (1994) Bioorg. Med. Chem. Lett. 4:2929-2934; Metelev U.S. Pat. No. 5,652,355; Metelev & Agrawal U.S. Pat. No. 6,143,881; Metelev& Agrawal U.S. Pat. No. 6,346,614; Metelev & Agrawal U.S. Pat. No. 6,683,167, Metelev & Agrawal U.S. Pat. No. 7,045,609).

Other approaches to improve stability and retain specificity and biologic activity of antisense oligonucleotides utilized triplex forming, polypyrimidine oligonucleotides that bind to double-stranded DNA or RNA targets. Polypyrimidine oligonucleotides can bind to duplex DNA in the major groove through Hoogsteen hydrogen bonding and form triplex structures containing one polypurine and two polypyrimidine strands with T:A-T and C:G-C⁺ base triplets (Moser, H. E. and Dervan, P. B. (1987) Science 238, 645-650; Cooney, et al (1988) Science 241, 456-459). Intramolecular triplexes are also formed when the DNA homopurine and homopryrimidine strands melt and refold (Vasqueza, K. M. and Wilson, J. H. (1998) Trends Bioche. Sci. 23, 4-9). The presence of a third strand introduces severe restrictions in the flexibility of the DNA, changing its ability to recognize specific proteins along the major groove (Shields, G. C., et al. (1997) Am. Chem. Soc., 119, 7463-7469; Jimenez-Garcia, E., et al. (1998) J. Biol. Chem. 273, 24640-24648, resulting in an inhibition of transcription and ultimately reduced gene expression. Oligonucleotides that can sequence-specifically bind to double-stranded DNA or RNA can act as transcriptional/translational regulators and offered a promising antigene/antisense strategy to control the regulation of gene expression (Giovannangeli, C. and Helene, C. (1997) Antisense Nucleic Acid Drug Dev., 413; Giovannangeli, C., et al. (1996) Biochemistry 35, 10539; Maher, L. J., et al. (1992) Biochemistry 31, 70). However, the conditions for forming stable triplexes are problematic because of limited base recognition and the non-physiologic acidic pH conditions required for protonation of cytosines in the triplex-forming oligonucleotides.

In an attempt to form such stable triplexes, polypyrimidine oligonucleotides with inverted polarity linked via a linker (i.e. one sequence having polarity 5′→3′ followed by another sequence with 3′→5′ polarity, or vice versa) have been described (Froehler, U.S. Pat. No. 5,399,676; Froehler U.S. Pat. No. 5,527,899; Froehler U.S. Pat. No. 5,721,218). In such inverted polarity oligonucleotides, the sequence on one side of the inversion binds to polypurine strand of a duplex according to the triple helix code and the sequence on the other side will bind to the adjacently located polypurine site in the opposite strand of the duplex (FIG. 1A). In this manner triple helix recognition can be extended by switching recognition from one strand of the duplex to the other and then back again, if desired and such target sequence stretch is available. In addition, these oligonucleotides may also form D-loops with the duplex as shown in FIG. 1B. In this situation, the region of the first polarity may form triplex, while the inverted portion displaces a section of one strand of the duplex to result in a substitute duplex in the relevant region. As the switchback oligonucleotides are capable of significant duplex binding activity, these oligonucleotides may be useful to inactivate the disease causing and undesirable DNA or RNA that are in duplex form. However, the composition of the molecules is limited to polypyrimidine sequences targeting polypurine sites of double-stranded RNA or DNA.

Alternatively, strategies have been developed to target single stranded DNA and RNA by triple helix formation. One of the approaches is to target polypyrimidine DNA or RNA single strands with foldback triplex-forming oligonucleotides with inverted polarity (Kandimalla, E. R., et al. (1995) J. Am. Chem. Soc. 117, 6416-6417; Kandimalla, E. R., and Agrawal, S. (1996) Biochemistry 35, 15332). In such foldback triplex-forming oligonucleotides, a polypyrimidine oligonucleotide and its complementary polypurine strand are attached through 3′-3′ attachment or 5′-5′-attachment. Such oligonucleotides containing complementary sequences attached through 3′-3′ or 5′-5′ linkages form parallel-stranded duplexes through Hoogsteen or reverse Hoogsteen base pairing. When a complementary polypyrimidine strand is available, they form triple helical structures (FIG. 2).

Despite considerable efforts, the efforts to improve the stability and maintain target recognition, without off-target effects has not generally produced oligonucleotides that would be perceived as having clinical utility. Thus, the existing antisense-based technologies leave open the challenge of creating compounds that are biologically stable, target specific, and efficient inhibitors of gene expression. New approaches are therefore needed.

BRIEF SUMMARY OF THE INVENTION

The present invention is directed to compounds, compositions, and methods useful for modulating miRNA activity using oligonucleotide-based compounds comprising two or more single stranded antisense oligonucleotides that are linked through their 5′-ends to allow the presence of two or more accessible 3′-ends, which effectively inhibit or decrease miRNA activity. Surprisingly, the present inventors have discovered that such oligonucleotide compounds are more effective than non-linked antisense oligonucleotides.

In a first aspect, the invention provides novel synthetic oligonucleotide-based compounds comprising two or more oligonucleotides that are complementary to one or more miRNA sequence, wherein the oligonucleotides are linked through their 5′ ends to allow the presence of two or more accessible 3′-ends, and specifically hybridize to and inhibit the activity of the one or more miRNA sequence.

In as second aspect, the invention provides for pharmaceutical compositions. These compositions may comprise any synthetic oligonucleotide-based compounds according to the first aspect in a pharmaceutically or physiologically acceptable carrier.

In a third aspect, the invention provides a method for inhibiting miRNA activity, the method comprising contacting a cell with a synthetic oligonucleotide-based compound according to the first aspect of the invention.

In a fourth aspect, the invention provides a method for inhibiting miRNA activity in a mammal, the method comprising administering to the mammal a synthetic oligonucleotide-based compound according to the first aspect of the invention.

In a fifth aspect, the invention provides a method for inhibiting a response mediated by a miRNA in a mammal through administration of a synthetic oligonucleotide-based compound according to the first aspect of the invention wherein the oligonucleotides are complementary to one or more miRNA sequence.

In a sixth aspect, the invention provides a method for inhibiting a response mediated by a miRNA in a mammal though administration of a synthetic oligonucleotide-based compound according to the first aspect of the invention wherein the oligonucleotides are complementary to one or more miRNA sequence in combination with an antagonist of RISC activity.

In a seventh aspect, the invention provides methods for inhibiting miRNA activity in a mammal, such methods comprising administering to the mammal an oligonucleotide-based compound according to the invention. In some embodiments, the mammal is a human. In some preferred embodiments, the oligonucleotide-based compound according to the invention is administered to a mammal in need of inhibiting its miRNA-mediated response.

In an eighth aspect, the invention provides methods for therapeutically treating a patient having a disease or disorder, such methods comprising administering to the patient an oligonucleotide-based compound according to the invention in a therapeutically effective amount. In various embodiments, the disease or disorder to be treated is cancer, an autoimmune disorder, infectious disease, airway inflammation, inflammatory disorders, skin disorder, allergy, asthma or a disease caused by a pathogen. Pathogens include, without limitation, bacteria, parasites, fungi, viruses, viroids, and prions.

In a ninth aspect, the invention provides methods for preventing a disease or disorder, such methods comprising administering to a subject at risk for developing the disease or disorder an oligonucleotide-based compound according to the invention in a pharmaceutically effective amount. In various embodiments, the disease or disorder to be prevented is cancer, an autoimmune disorder, airway inflammation, inflammatory disorders, infectious disease, allergy, asthma or a disease caused by a pathogen. Pathogens include, without limitation, bacteria, parasites, fungi, viruses, viroids, and prions.

In a tenth aspect the invention provides a method of preventing or treating a disorder, such methods comprises isolating cells capable of producing cytokines or chemokines including, but not limited to, immune cells, T-regulatory cells, B-cells, PBMCs, pDCs, and lymphoid cells; culturing such cells under standard cell culture conditions, treating such cells ex vivo with an oligonucleotide-based compound according to the first aspect of the invention such that the isolated cells produce or secrete decreased levels of cytokines or chemokines, and administering or re-administering the treated cells to a patient in need of therapy to inhibit cytokines and/or chemokines for the prevention and/or treatment of disease. This aspect of the invention would be in accordance with standard adoptive cellular immunotherapy techniques to produce activated immune cells.

In an eleventh aspect, the invention provides a composition comprising a compound according to the first aspect of the invention and one or more vaccines, antigens, antibodies, cytotoxic agents, chemotherapeutic agents (both traditional chemotherapy and modern targeted therapies), kinase inhibitors, allergens, antibiotics, agonist, antagonist, antisense oligonucleotides, ribozymes, RNAi molecules, siRNA molecules, miRNA molecules, aptamers, proteins, gene therapy vectors, DNA vaccines, adjuvants, co-stimulatory molecules or combinations thereof.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic description of switchback triplex-forming (A) and D-loop (B) modes of binding oligonucleotides with inverted polarity.

FIG. 2 is a schematic representation of parallel-stranded hairpin modes of oligonucleotides containing purine-pyrimidine strands attached covalently either 3′-3′ or 5′-5′ ends.

FIG. 3 is a schematic description of the antisense mode of binding of the oligonucleotide-based compounds according to the invention.

FIG. 4A is a synthetic scheme for the linear synthesis of antisense oligonucleotides of the invention. DMTr=4,4′-dimethoxytrityl; CE=cyanoethyl.

FIG. 4B is synthetic scheme for the parallel synthesis of antisense oligonucleotides of the invention. DMTr=4,4′-dimethoxytrityl; CE=cyanoethyl.

FIGS. 5A and 5B depict the antisense activity of exemplary antisense oligonucleotides according to the invention in HEK293 cells expressing murine TLR9. The data demonstrate the ability of antisense oligonucleotides according to the invention to inhibit TLR9 agonist activity in cells cultured and treated according to Example 2.

FIG. 5C depicts the antisense activity of exemplary antisense oligonucleotides according to the invention in HEK293 cells expressing murine TLR7. The data demonstrate the ability of antisense oligonucleotides according to the invention to inhibit TLR7 agonist activity in cells cultured and treated according to Example 2.

FIG. 5D depicts the antisense activity of exemplary antisense oligonucleotides according to the invention in HEK293 cells expressing murine MyD88. The data demonstrate the ability of antisense oligonucleotides according to the invention to inhibit MyD88 agonist activity in cells cultured and treated according to Example 2.

FIG. 6 depicts the antisense activity of exemplary antisense oligonucleotides according to the invention in mouse splenocytes. The data demonstrate the ability of antisense oligonucleotides according to the invention to inhibit TLR9 mRNA translation, or protein synthesis, in splenocytes treated according to Example 2.

FIG. 7 depicts the antisense activity of exemplary antisense oligonucleotides according to the invention in human PBMCs. The data demonstrate the ability of antisense oligonucleotides according to the invention to inhibit TLR9 mRNA translation, or protein synthesis, in human PBMCs treated according to Example 2.

FIGS. 8A and 8B depict the activity of exemplary antisense oligonucleotides according to the invention to inhibit TLR9-induced IL-12 following in vivo administration according to Example 3. The data demonstrate that administration of an exemplary TLR9 antisense oligonucleotide according to the invention can cause down-regulation of TLR9 expression in vivo and prevent the induction of IL-12 by a TLR9 agonist. More generally, the data demonstrate the ability of a TLR9 antisense oligonucleotide according to the invention to inhibit the induction of pro-inflammatory cytokines by a TLR9 agonist.

FIG. 8C depicts the duration of in vivo activity of exemplary antisense oligonucleotides according to the invention to inhibit MyD88-induced IL-12 following in vivo administration according to Example 3. The data demonstrate that administration of an exemplary MyD88 antisense oligonucleotide according to the invention can cause down-regulation of MyD88 expression in vivo and prevent the induction of IL-12 by a TLR9 agonist for a longer duration than either linear antisense oligonucleotides or 3′-3′ linked antisense oligonucleotides. More generally, the data demonstrate the ability of a MyD88 antisense oligonucleotide according to the invention to inhibit the induction of pro-inflammatory cytokines by a TLR agonist.

FIG. 9 depicts the activity of exemplary antisense oligonucleotides according to the invention to inhibit TLR9-induced IL-12 in a dose dependent manner following in vivo administration according to Example 3. The data demonstrate that in vivo administration of a TLR9 antisense oligonucleotide according to the invention can cause down-regulation of TLR9 expression in vivo in a dose dependent manner and prevent the induction of IL-12 by a TLR9 agonist. More generally, the data demonstrate the ability of a TLR9 antisense oligonucleotide according to the invention to selectively inhibit the induction of pro-inflammatory cytokines by a TLR9 agonist.

FIG. 10 depicts the activity of exemplary antisense oligonucleotides according to the invention to inhibit TLR9-induced IL-12 in a time dependent manner following in vivo administration according to Example 3. The data demonstrate that in vivo administration of a TLR9 antisense oligonucleotide according to the invention can cause down-regulation of TLR9 expression in vivo in a time dependent manner and prevent the induction of IL-12 by a TLR9 agonist for an extended period of time. More generally, the data demonstrate the ability of a TLR9 antisense oligonucleotide according to the invention to inhibit the induction of pro-inflammatory cytokines by a TLR9 agonist in a time dependent manner.

FIGS. 11A, 11B and 11C depict the antisense activity of exemplary antisense oligonucleotides according to the invention in murine J774 cells. The data demonstrate the ability of antisense oligonucleotides according to the invention to inhibit TLR9 mRNA, transcription, translation, or protein synthesis, in murine J774 cells treated according to Example 2.

FIG. 11D depicts the antisense activity of exemplary antisense oligonucleotides according to the invention in human HeLa cells. The data demonstrate the ability of antisense oligonucleotides according to the invention to inhibit VEGF mRNA transcription in human HeLa cells treated according to Example 2.

FIG. 12 depicts the antisense activity of exemplary antisense oligonucleotides according to the invention in human B cells. The data demonstrate the ability of antisense oligonucleotides according to the invention to inhibit TLR9 mRNA translation, or protein synthesis, in human B cells treated according to Example 2.

FIG. 13 depicts the antisense activity of exemplary antisense oligonucleotides according to the invention in human pDCs. The data demonstrate the ability of antisense oligonucleotides according to the invention to inhibit TLR9 mRNA translation, or protein synthesis, in human pDCs treated according to Example 2.

FIG. 14 depicts the activity of exemplary antisense oligonucleotides according to the invention to inhibit TLR9-induced IL-12 following in vivo administration according to Example 3. The data demonstrate that in vivo administration of an exemplar TLR9 antisense oligonucleotide according to the invention can cause down-regulation of TLR9 expression in vivo and prevent the induction of IL-12 by a TLR9 agonist. More generally, the data demonstrate the ability of a TLR9 antisense oligonucleotide according to the invention to inhibit the induction of pro-inflammatory cytokines by a TLR9 agonist.

FIG. 15 depicts the antisense activity of exemplary antisense oligonucleotides according to the invention in HEK293 cells expressing mouse TLR7. The data demonstrate the ability of antisense oligonucleotides according to the invention to inhibit TLR7 agonist activity in cells cultured and treated according to Example 2.

FIG. 16 depicts the selective binding and cleavage of exemplary antisense oligonucleotides according to the invention treated according to Example 4. In FIG. 16, Lane 1 is substrate alone; Lane 2 is T1 nuclease; Lane 3 is 5′-AAUGCUUGUCUGUGCAGUCC-3′ (SEQ ID NO. 28); Lane 4 is 5′-AAUGCUUGUCUGUGCAGUCC-X-CCUGACGUGUCUGUUCGUAA-5′; Lane 5 is 3′-CCUGACGUGUCUGUUCGUAA-X-AAUGCUUGUCUGUGCAGUCC-3′ (SEQ ID 21); Lane 6 is 5′-AAUGCUUGUCUGUGCAGUCC-AAUGCUUGUCUGUGCAGUCC-3′; Lane 7 is 5′-CUGUCoAoAoAoUoGoCoUoUoGoUoCoUoGoUoGoCoAoGoUoCoCoACGAU-3′ (SEQ ID NO. 29); Lane 8 is dsRNA; and Lane 9 is 20-mer DNA antisense; wherein all sequences have phosphorothioate backbone except where indicated with an “o” (phosphodiester linkage); underlined nucleotides indicate 2′-O-methylribonucleotides. The data demonstrate that oligonucleotides according to the invention provide an optimal structure for binding and cleavage by proteins and enzymes associated with RNAi-mediated inhibition of gene expression.

FIG. 17 depicts the activity of exemplary GSO molecules directed to miR-21. Cells were treated according to Example 5. The data show that GSO molecules according to the invention that are directed to miR-21 effectively decrease the relative amount of miR-21 miRNA present following administration of the miR-21 GSO. The data more generally demonstrate that GSOs directed to a miRNA target can effectively reduce the quantity of the target miRNA.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The invention relates to the therapeutic and prophylactic use of novel antisense oligonucleotides to down-regulate gene expression. Such molecules are useful, for example, in providing compositions for modulation of gene expression or for treating and/or preventing diseases and/or conditions that are capable of responding to modulation of gene expression in patients, subjects, animals or organisms.

The patents and publications cited herein reflect the level of knowledge in the art and are hereby incorporated by reference in their entirety. Any conflict between the teachings of these patents and publications and this specification shall be resolved in favor of the latter.

The objects of the present invention, the various features thereof, as well as the invention itself may be more fully understood from the following description, when read together with the accompanying drawings in which the following terms have the ascribed meaning.

The term “2′-O-substituted” means substitution of the 2′ position of the pentose moiety with an —O— lower alkyl group containing 1-6 saturated or unsaturated carbon atoms (for example, but not limited to, 2′-O-methyl), or with an —O-aryl or allyl group having 2-6 carbon atoms, wherein such alkyl, aryl or allyl group may be unsubstituted or may be substituted, (for example, with 2′-O-methoxyethyl, ethoxy, methoxy, halo, hydroxyl, trifluoromethyl, cyano, nitro, acyl, acyloxy, alkoxy, carboxyl, carbalkoxyl, or amino groups); or with a hydroxyl, an amino or a halo group, but not with a 2′-H group. In some embodiments the oligonucleotides of the invention include four or five 2′-O-alky nucleotides at their 5′ terminus, and/or four or five 2′-O-alky nucleotides at their 3′ terminus.

The term “3′”, when used directionally, generally refers to a region or position in a polynucleotide or oligonucleotide 3′ (toward the 3′ end of the nucleotide) from another region or position in the same polynucleotide or oligonucleotide.

The term “3′ end” generally refers to the 3′ terminal nucleotide of the component oligonucleotides. “Two or more oligonucleotides linked at their 3′ ends” generally refers to a linkage between the 3′ terminal nucleotides of the oligonucleotides which may be directly via 5′, 3′ or 2′ hydroxyl groups, or indirectly, via a non-nucleotide linker. Such linkages may also be via a nucleoside, utilizing both 2′ and 3′ hydroxyl positions of the nucleoside. Such linkages may also utilize a functionalized sugar or nucleobase of a 3′terminal nucleotide.

The term “5′”, when used directionally, generally refers to a region or position in a polynucleotide or oligonucleotide 5′ (toward the 5′ end of the nucleotide) from another region or position in the same polynucleotide or oligonucleotide.

The term “5′ end” generally refers to the 5′ terminal nucleotide of the component oligonucleotides. “Two or more single-stranded antisense oligonucleotides linked at their 5′ ends” generally refers to a linkage between the 5′ terminal nucleotides of the oligonucleotides which may be directly via 5′, 3′ or 2′ hydroxyl groups, or indirectly, via a non-nucleotide linker. Such linkages may also be via a nucleoside, utilizing both 2′ and 3′ hydroxyl positions of the nucleoside. Such linkages may also utilize a functionalized sugar or nucleobase of a 5′terminal nucleotide.

The term “about” generally means that the exact number is not critical. Thus, oligonucleotides having one or two fewer nucleoside residues, or from one to several additional nucleoside residues are contemplated as equivalents of each of the embodiments described above.

The term “accessible” generally means when related to a compound according to the invention, that the relevant portion of the molecule is able to be recognized by the cellular components necessary to elicit an intended response to the compound.

The term “agonist” generally refers to a substance that binds to a receptor of a cell and induces a response. An agonist often mimics the action of a naturally occurring substance such as a ligand.

The term “antagonist” generally refers to a substance that attenuates the effects of an agonist or ligand.

The term “airway inflammation” generally includes, without limitation, inflammation in the respiratory tract caused by allergens, including asthma.

The term “allergen” generally refers to an antigen or antigenic portion of a molecule, usually a protein, which elicits an allergic response upon exposure to a subject. Typically the subject is allergic to the allergen as indicated, for instance, by the wheal and flare test or any method known in the art. A molecule is said to be an allergen even if only a small subset of subjects exhibit an allergic (e.g., IgE) immune response upon exposure to the molecule.

The term “allergy” generally includes, without limitation, food allergies, respiratory allergies and skin allergies.

The term “antigen” generally refers to a substance that is recognized and selectively bound by an antibody or by a T cell antigen receptor. Antigens may include but are not limited to peptides, proteins, lipids, carbohydrates, nucleosides, nucleotides, nucleic acids, and combinations thereof. Antigens may be natural or synthetic and generally induce an immune response that is specific for that antigen.

The term “autoimmune disorder” generally refers to disorders in which “self” antigen undergo attack by the immune system. Such term includes, without limitation, lupus erythematosus, multiple sclerosis, type I diabetes mellitus, irritable bowel syndrome, Chron's disease, rheumatoid arthritis, septic shock, alopecia universalis, acute disseminated encephalomyelitis, Addison's disease, ankylosing spondylitis, antiphospholipid antibody syndrome, autoimmune hemolytic anemia, autoimmune hepatitis, Bullous pemphigoid, chagas disease, chronic obstructive pulmonary disease, hydrox disease, dermatomyositis, endometriosis, Goodpasture's syndrome, Graves' disease, Guillain-Barré syndrome, Hashimoto's disease, hidradenitis suppurativa, idiopathic thrombocytopenic purpura, interstitial cystitis, morphea, myasthenia gravis, narcolepsy, neuromyotonia, pemphigus, pernicious anaemia, polymyositis, primary biliary cirrhosis, schizophrenia, Sjogren's syndrome, temporal arteritis (“giant cell arteritis”), vasculitis, vitiligo, vulvodynia and Wegener's granulomatosis autoimmune asthma, septic shock and psoriasis.

The term “biologic instability” generally refers to a molecule's ability to be degraded and subsequently inactivated in vivo. For oligonucleotides, such degradation results from exonuclease activity and/or endonuclease activity, wherein exonuclease activity refers to cleaving nucleotides from the 3′ or 5′ end of an oligonucleotide, and endonuclease activity refers to cleaving phosphodiester bonds at positions other than at the ends of the oligonucleotide.

The term “cancer” generally refers to, without limitation, any malignant growth or tumor caused by abnormal or uncontrolled cell proliferation and/or division. Cancers may occur in humans and/or mammals and may arise in any and all tissues. Treating a patient having cancer may include administration of a compound, pharmaceutical formulation or vaccine according to the invention such that the abnormal or uncontrolled cell proliferation and/or division, or metastasis is affected.

The term “carrier” generally encompasses any excipient, diluent, filler, salt, buffer, stabilizer, solubilizer, oil, lipid, lipid containing vesicle, microspheres, liposomal encapsulation, or other material for use in pharmaceutical formulations. It will be understood that the characteristics of the carrier, excipient or diluent will depend on the route of administration for a particular application. The preparation of pharmaceutically acceptable formulations containing these materials is described in, for example, Remington's Pharmaceutical Sciences, 18^(th) Edition, ed. A. Gennaro, Mack Publishing Co., Easton, Pa., 1990.

The term “co-administration” or “co-administered” generally refers to the administration of at least two different substances sufficiently close in time to modulate an immune response. Co-administration refers to simultaneous administration, as well as temporally spaced order of up to several days apart, of at least two different substances in any order, either in a single dose or separate doses.

The term “in combination with” generally means administering an oligonucleotide-based compound according to the invention and another agent useful for treating the disease or condition that does not abolish the activity of the compound in the course of treating a patient. Such administration may be done in any order, including simultaneous administration, as well as temporally spaced order from a few seconds up to several days apart. Such combination treatment may also include more than a single administration of the compound according to the invention and/or independently the other agent. The administration of the compound according to the invention and the other agent may be by the same or different routes.

The term “individual” or “subject” or “patient” generally refers to a mammal, such as a human.

The term “kinase inhibitor” generally refers to molecules that antagonize or inhibit phosphorylation-dependent cell signaling and/or growth pathways in a cell. Kinase inhibitors may be naturally occurring or synthetic and include small molecules that have the potential to be administered as oral therapeutics. Kinase inhibitors have the ability to rapidly and specifically inhibit the activation of the target kinase molecules. Protein kinases are attractive drug targets, in part because they regulate a wide variety of signaling and growth pathways and include many different proteins. As such, they have great potential in the treatment of diseases involving kinase signaling, including cancer, cardiovascular disease, inflammatory disorders, diabetes, macular degeneration and neurological disorders. A non-limiting example of a kinase inhibitor is sorafenib.

The term “linear synthesis” generally refers to a synthesis that starts at one end of an oligonucleotide and progresses linearly to the other end. Linear synthesis permits incorporation of either identical or non-identical (in terms of length, base composition and/or chemical modifications incorporated) monomeric units into an oligonucleotide.

The term “mammal” is expressly intended to include warm blooded, vertebrate animals, including, without limitation, humans, non-human primates, rats, mice, cats, dogs, horses, cattle, cows, pigs, sheep and rabbits.

The term “nucleoside” generally refers to compounds consisting of a sugar, usually ribose, deoxyribose, pentose, arabinose or hexose, and a purine or pyrimidine base.

The term “nucleotide” generally refers to a nucleoside comprising a phosphorous-containing group attached to the sugar.

The term “modified nucleoside” or “nucleotide derivative” generally is a nucleoside that includes a modified heterocyclic base, a modified sugar moiety, or any combination thereof. In some embodiments, the modified nucleoside or nucleotide derivative is a non-natural pyrimidine or purine nucleoside, as herein described. For purposes of the invention, a modified nucleoside or nucleotide derivative, a pyrimidine or purine analog or non-naturally occurring pyrimidine or purine can be used interchangeably and refers to a nucleoside that includes a non-naturally occurring base and/or non-naturally occurring sugar moiety. For purposes of the invention, a base is considered to be non-natural if it is not guanine, cytosine, adenine, thymine or uracil and a sugar is considered to be non-natural if it is not β-ribo-furanoside or 2′-deoxyribo-furanoside.

The term “modified oligonucleotide” as used herein describes an oligonucleotide in which at least two of its nucleotides are covalently linked via a synthetic linkage, i.e., a linkage other than a phosphodiester linkage between the 5′ end of one nucleotide and the 3′ end of another nucleotide in which the 5′ nucleotide phosphate has been replaced with any number of chemical groups. The term “modified oligonucleotide” also encompasses 2′-0,4′-C-methylene-b-D-ribofuranosyl nucleic acids, arabinose nucleic acids, substituted arabinose nucleic acids, hexose nucleic acids, peptide nucleic acids, morpholino, and oligonucleotides having at least one nucleotide with a modified base and/or sugar, such as a 2′-O-substituted, a 5-methylcytosine and/or a 3′-O-substituted ribonucleotide.

The term “nucleic acid” encompasses a genomic region or an RNA molecule transcribed therefrom. In some embodiments, the nucleic acid is mRNA.

The term “linker” generally refers to any moiety that can be attached to an oligonucleotide by way of covalent or non-covalent bonding through a sugar, a base, or the backbone. The non-covalent linkage may be, without limitation, electrostatic interactions, hydrophobic interactions, π-stacking interactions, hydrogen bonding and combinations thereof. Non-limiting examples of such non-covalent linkage includes Watson-Crick base pairing, Hoogsteen base pairing, and base stacking. The linker can be used to attach two or more nucleosides or can be attached to the 5′ and/or 3′ terminal nucleotide in the oligonucleotide. Such linker can be either a non-nucleotide linker or a nucleoside linker.

The term “non-nucleotide linker” generally refers to a chemical moiety, other than a linkage directly between two nucleotides that can be attached to an oligonucleotide by way of covalent or non-covalent bonding. Preferably such non-nucleotide linker is from about 2 angstroms to about 200 angstroms in length, and may be either in a cis or trans orientation.

The term “internucleotide linkage” generally refer to a chemical linkage to join two nucleosides through their sugars (e.g. 3′-3′,2′-3′,2′-5′,3′-5′,5′-5′) consisting of a phosphorous atom and a charged, or neutral group (e.g., phosphodiester, phosphorothioate, phosphorodithioate or methylphosphonate) between adjacent nucleosides.

The term “oligonucleotide” refers to a polynucleoside formed from a plurality of linked nucleoside units, which may include, for example, deoxyribonucleotides or ribonucleotides, synthetic or natural nucleotides, phosphodiester or modified linkages, natural bases or modified bases natural sugars or modified sugars, or combinations of these components. The nucleoside units may be part of viruses, bacteria, cell debris or oligonucleotide-based compositions (for example, siRNA and microRNA). Such oligonucleotides can also be obtained from existing nucleic acid sources, including genomic or cDNA, but are preferably produced by synthetic methods. In certain embodiments each nucleoside unit includes a heterocyclic base and a pentofuranosyl, trehalose, arabinose, 2′-deoxy-2′-substituted nucleoside, 2′-deoxy-2′-substituted arabinose, 2′-O-substituted arabinose or hexose sugar group. The nucleoside residues can be coupled to each other by any of the numerous known internucleoside linkages. Such internucleoside linkages include, without limitation, phosphodiester, phosphorothioate, phosphorodithioate, methylphosphonate, alkylphosphonate, alkylphosphonothioate, phosphotriester, phosphoramidate, siloxane, carbonate, carboalkoxy, acetamidate, carbamate, morpholino, borano, thioether, bridged phosphoramidate, bridged methylene phosphonate, bridged phosphorothioate, and sulfone internucleoside linkages. The term “oligonucleotide” also encompasses polynucleosides having one or more stereospecific internucleoside linkage (e.g., (R_(p))- or (S_(p))-phosphorothioate, alkylphosphonate, or phosphotriester linkages). As used herein, the terms “oligonucleotide” and “dinucleotide” are expressly intended to include polynucleosides and dinucleosides having any such internucleoside linkage, whether or not the linkage comprises a phosphate group. In certain exemplary embodiments, these internucleoside linkages may be phosphodiester, phosphorothioate or phosphorodithioate linkages, or combinations thereof. In exemplary embodiments, the nucleotides of the synthetic oligonucleotides are linked by at least one phosphorothioate internucleoside linkage. The phosphorothioate linkages may be mixed Rp and Sp enantiomers, or they may be stereoregular or substantially stereoregular in either Rp or Sp form (see Iyer et al. (1995) Tetrahedron Asymmetry 6:1051-1054). In certain embodiments, one or more of the oligonucleotides within the antisense compositions of the invention contain one or more 2′-O,4′-C-methylene-b-D-ribofuranosyl nucleic acids, wherein the ribose is modified with a bond between the 2′ and 4′ carbons, which fixes the ribose in the 3′-endo structural conformation.

The phrase “an oligonucleotide that is complementary to a single-stranded RNA sequence” and the like, means that the oligonucleotide forms a sufficient number of hydrogen bonds through Watson-Crick interactions of its nucleobases with nucleobases of the single-stranded RNA sequence to form a double helix with the single-stranded RNA sequence under physiological conditions. This is in contrast to oligonucleotides that form a triple helix with a double-stranded DNA or RNA through Hoogsteen hydrogen bonding.

The term “complementary” is intended to mean an oligonucleotide that binds to the nucleic acid sequence under physiological conditions, for example, by Watson-Crick base pairing (interaction between oligonucleotide and single-stranded nucleic acid) or by Hoogsteen base pairing (interaction between oligonucleotide and double-stranded nucleic acid) or by any other means, including in the case of an oligonucleotide, binding to RNA and causing pseudoknot formation. Binding by Watson-Crick or Hoogsteen base pairing under physiological conditions is measured as a practical matter by observing interference with the function of the nucleic acid sequence.

The term “peptide” generally refers to oligomers or polymers of amino acids that are of sufficient length and composition to affect a biological response, for example, antibody production or cytokine activity whether or not the peptide is a hapten. The term “peptide” may include modified amino acids (whether or not naturally or non-naturally occurring), where such modifications include, but are not limited to, phosphorylation, glycosylation, pegylation, lipidization, and methylation.

The term “pharmaceutically acceptable” means a non-toxic material that does not interfere with the effectiveness of a compound according to the invention or the biological activity of a compound according to the invention.

The term “physiologically acceptable” refers to a non-toxic material that is compatible with a biological system such as a cell, cell culture, tissue, or organism. Preferably, the biological system is a living organism, such as a mammal, particularly a human.

The term “prophylactically effective amount” generally refers to an amount sufficient to prevent or reduce the development of an undesired biological effect.

The term “therapeutically effective amount” or “pharmaceutically effective amount” generally refers to an amount sufficient to affect a desired biological effect, such as a beneficial result, including, without limitation, prevention, diminution, amelioration or elimination of signs or symptoms of a disease or disorder. Thus, the total amount of each active component of the pharmaceutical composition or method is sufficient to show a meaningful patient benefit, for example, but not limited to, healing of chronic conditions characterized by immune stimulation. Thus, a “pharmaceutically effective amount” will depend upon the context in which it is being administered. A pharmaceutically effective amount may be administered in one or more prophylactic or therapeutic administrations. When applied to an individual active ingredient, administered alone, the term refers to that ingredient alone. When applied to a combination, the term refers to combined amounts of the active ingredients that result in the therapeutic effect, whether administered in combination, serially or simultaneously.

The term “treatment” generally refers to an approach intended to obtain a beneficial or desired result, which may include alleviation of symptoms, or delaying or ameliorating a disease progression.

The term “gene expression” generally refers to process by which information from a gene is used in the synthesis of a functional gene product, which may be a protein. The process may involve transcription, RNA splicing, translation, and post-translational modification of a protein, and may include mRNA, preRNA, ribosomal RNA, and other templates for protein synthesis.

In a first aspect, the invention provides novel oligonucleotide-based compounds comprising two or more single-stranded antisense oligonucleotides linked at their 5′ ends, wherein the compounds have two or more accessible 3′ ends. The linkage at the 5′ ends of the component oligonucleotides is independent of the other oligonucleotide linkages and may be directly via 5′, 3′ or 2′ hydroxyl groups, or indirectly, via a non-nucleotide linker or a nucleoside, utilizing either the 2′ or 3′ hydroxyl positions of the nucleoside. Linkages may also utilize a functionalized sugar or nucleobase of a 5′ terminal nucleotide.

Oligonucleotide-based compounds according to the invention comprise two identical or different sequences conjugated at their 5′-5′ ends via a phosphodiester, phosphorothioate or non-nucleoside linker (FIG. 3). Such compounds comprise at least one oligonucleotide having 15 to 22 nucleotides that are complementary to specific portions or all of miRNA targets of interest for antisense down regulation of miRNA activity. Oligonucleotide-based compounds according to the invention that comprise identical sequences are able to bind to a specific miRNA via Watson-Crick hydrogen bonding interactions and inhibit miRNA activity (FIG. 3). Oligonucleotide-based compounds according to the invention that comprise different sequences are able to bind to two or more different regions of one or more miRNA target and inhibit protein expression. Such compounds are comprised of heteronucleotide sequences complementary to target miRNA and form stable duplex structures through Watson-Crick hydrogen bonding. Surprisingly, such sequences containing two free 3′-ends (5′-5′-attached antisense) are more potent inhibitors of miRNA activity than those containing a single free 3′-end or no free 3′-end.

Oligonucleotide-based compounds according to the invention are useful in treating and/or preventing diseases wherein inhibiting miRNA activity would be beneficial. Oligonucleotide-based compounds according to the invention include, but are not limited to, antisense oligonucleotides comprising naturally occurring nucleotides, modified nucleotides, modified oligonucleotides and/or backbone modified oligonucleotides. However, antisense oligonucleotides that inhibit the activity of mRNA may produce undesired biological effects, including but not limited to insufficient antisense activity, inadequate bioavailability, suboptimal pharmacokinetics or pharmacodynamics, unintended immune stimulation, off target activity, and biologic instability. The optimal design of an antisense oligonucleotide according to the invention requires many considerations beyond simple design of a molecule that is complementary to the target miRNA sequence. Thus, preparation of antisense oligonucleotides according to the invention is intended to incorporate changes necessary to limit secondary structure interference with antisense activity, enhance the oligonucleotide's target specificity, minimize interaction with binding or competing factors (for example, proteins), optimize cellular uptake, bioavailability, pharmacokinetics, and pharmacodynamics, and/or inhibit, prevent or suppress immune cell activation.

The general structure of the oligonucleotide-based compounds of the invention may be described by the following formula.

3′-Nn . . . N1N2N3N4-5′-L-5′-N8N7N6N5 . . . Nm-3′  (Formula I)

Wherein L is a nucleotide linker or non-nucleotide linker; N1-N8, at each occurrence, is independently a nucleotide or nucleotide derivative; Nm and Nn, at each occurrence, are independently a nucleotide or nucleotide derivative; and wherein m and n are independently numbers from 0 to about 40. Representative non-nucleotide linkers are set forth in Table 1.

TABLE 1 Representative Non-Nucleotide Linkers

In some embodiments, the small molecule linker is glycerol or a glycerol homolog of the formula HO—(CH₂)_(o)—CH(OH)—(CH₂)_(p)—OH, wherein o and p independently are integers from 1 to about 6, from 1 to about 4 or from 1 to about 3. In some other embodiments, the small molecule linker is a derivative of 1,3-diamino-2-hydroxypropane. Some such derivatives have the formula HO—(CH₂)₁₂—C(O)NH—CH₂—CH(OH)—CH₂—NHC(O)—(CH₂)_(m)—OH, wherein m is an integer from 0 to about 10, from 0 to about 6, from 2 to about 6 or from 2 to about 4.

Some non-nucleotide linkers according to the invention permit attachment of more than two oligonucleotide-based compounds of the invention. For example, the small molecule linker glycerol has three hydroxyl groups to which such oligonucleotides may be covalently attached. Some oligonucleotide-based compounds of the invention, therefore, comprise two or more oligonucleotides linked to a nucleotide or a non-nucleotide linker. Such oligonucleotides according to the invention are referred to as being “branched”.

Oligonucleotide-based compounds according to the invention may comprise at least two linked antisense oligonucleotides with two or more free 3′ ends. Some of the ways in which two or more oligonucleotides can be linked are shown in Table 2.

TABLE 2 Oligoribonucleotide Formulas II-V

Formula II

Formula III

Formula IV

Formula V

In certain embodiments of Formulas II and/or V, L is a linker or a nucleotide linkage and Domain A and/or Domain B are antisense oligonucleotides that are designed to selectively hybridize to the same target RNA sequence or different target RNA sequences.

In certain embodiments of Formulas II, III, IV or V, L is a linker and Domain A and/or Domain B and/or Domain C are antisense oligonucleotides that are designed to selectively hybridize to the same miRNA sequence or different miRNA sequences. For example, in one embodiment, Domain A and/or Domain B and/or Domain C of Formulas II and/or III are antisense oligonucleotides that are designed to selectively hybridize to the same miRNA sequence. In this embodiment, Domain A and/or Domain B and/or Domain C can be designed to hybridize to the same region on the miRNA sequence or to different regions of the same miRNA sequence.

In a further embodiment of this aspect of the invention, Domain A, Domain B, and Domain C are independently RNA or DNA-based oligonucleotides. In certain aspects of this embodiment, the oligonucleotides comprise mixed backbone oligonucleotides.

In another embodiment, one or more of Domain A and/or Domain B and/or Domain C of Formula IV is an antisense oligonucleotide that is designed to selectively hybridize to one miRNA sequence and one or more of the remaining Domain A and/or Domain B and/or Domain C is an antisense oligonucleotide that is designed to selectively hybridized to a different miRNA sequence.

In another embodiments, one or more of Domain A, Domain B or Domain C of Formula IV is an antagonist of a cell-surface or intracellular receptor. In certain embodiments, the antagonist is a TLR antagonist.

In another embodiment, one or more of Domain A and/or Domain B and/or Domain C of Formula II, III, IV and/or V is an RNA-based oligonucleotide hybridized to a complimentary RNA-based oligonucleotide such that the domain comprises an siRNA molecule.

The component oligonucleotides of oligonucleotide-based compounds of the invention are at least 14 nucleotides in length, but are preferably 15 to 40 nucleotides long, preferably 15 to 22 or 20 to 30 nucleotides in length. Thus, the component oligonucleotides of the oligonucleotide-based compounds of the invention can independently be 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 or 40 nucleotides in length. These oligonucleotides can be prepared by the art recognized methods such as phosphoramidate or H-phosphonate chemistry which can be carried out manually or by an automated synthesizer. Representative synthetic approaches are shown in FIGS. 4A and 4B. The synthetic antisense oligonucleotides of the invention may also be modified in a number of ways without compromising their ability to hybridize to mRNA. Such modifications may include at least one internucleotide linkage of the oligonucleotide being an alkylphosphonate, phosphorothioate, phosphorodithioate, methylphosphonate, phosphate ester, alkylphosphonothioate, phosphoramidate, carbamate, carbonate, phosphate hydroxyl, acetamidate or carboxymethyl ester or a combination of these and other internucleotide linkages between the 5′ end of one nucleotide and the 3′ end of another nucleotide in which the 5′ nucleotide phosphodiester linkage has been replaced with any number of chemical groups.

The synthetic antisense oligonucleotides of the invention may comprise combinations of internucleotide linkages. For example, U.S. Pat. No. 5,149,797 describes traditional chimeric oligonucleotides having a phosphorothioate core region interposed between methylphosphonate or phosphoramidate flanking regions. Additionally, U.S. Pat. No. 5,652,356 discloses “inverted” chimeric oligonucleotides comprising one or more nonionic oligonucleotide region (e.g. alkylphosphonate and/or phosphoramidate and/or phosphotriester internucleoside linkage) flanked by one or more region of oligonucleotide phosphorothioate. Various synthetic antisense oligonucleotides with modified internucleotide linkages can be prepared according to standard methods. In certain embodiments, the phosphorothioate linkages may be mixed Rp and Sp enantiomers, or they may be made stereoregular or substantially stereoregular in either Rp or Sp form.

Other modifications of oligonucleotide-based compounds of the invention include those that are internal or at the end(s) of the oligonucleotide molecule and include additions to the molecule of the internucleoside phosphate linkages, such as cholesterol, cholesteryl, or diamine compounds with varying numbers of carbon residues between the amino groups and terminal ribose, deoxyribose and phosphate modifications which cleave, or crosslink to the opposite chains or to associated enzymes or other proteins which bind to the genome. Examples of such modified oligonucleotides include oligonucleotides with a modified base and/or sugar such as 2′-O,4′-C-methylene-b-D-ribofuranosyl, or arabinose instead of ribose, or a 3′,5′-substituted oligonucleotide having a sugar which, at both its 3′ and 5′ positions, is attached to a chemical group other than a hydroxyl group (at its 3′ position) and other than a phosphate group (at its 5′ position).

Other examples of modifications to sugars of the oligonucleotide-based compounds of the invention include modifications to the 2′ position of the ribose moiety which include but are not limited to 2′-O-substituted with an —O-alkyl group containing 1-6 saturated or unsaturated carbon atoms, or with an —O-aryl, or —O-allyl group having 2-6 carbon atoms wherein such —O-alkyl, —O-aryl or —O-allyl group may be unsubstituted or may be substituted, for example with halo, hydroxyl, trifluoromethyl, cyano, nitro, acyl, acyloxy, alkoxy, carboxy, carbalkoxyl or amino groups. None of these substitutions are intended to exclude the presence of other residues having native 2′-hydroxyl group in the case of ribose or 2′ H— in the case of deoxyribose.

The oligonucleotides-based compounds according to the invention can comprise one or more ribonucleotides. For example, U.S. Pat. No. 5,652,355 discloses traditional hybrid oligonucleotides having regions of 2′-O-substituted ribonucleotides flanking a DNA core region. U.S. Pat. No. 5,652,356 discloses an “inverted” hybrid oligonucleotide that includes an oligonucleotide comprising a 2′-O-substituted (or 2′ OH, unsubstituted) RNA region which is in between two oligodeoxyribonucleotide regions, a structure that “inverted relative to the “traditional” hybrid oligonucleotides. Non-limiting examples of particularly useful oligonucleotides of the invention have 2′-O-alkylated ribonucleotides at their 3′, 5′, or 3′ and 5′ termini, with at least four, and in some exemplary embodiments five, contiguous nucleotides being so modified. Non-limiting examples of 2′-O-alkylated groups include 2′-O-methyl, 2′-β-ethyl, 2′-O-propyl, 2′-O-butyls and 2′-O-methoxy-ethyl.

The oligonucleotide-based compounds of the invention may conveniently be synthesized using an automated synthesizer and phosphoramidite approach as schematically depicted in FIG. 4B, and further described in Example 1. In some embodiments, the oligonucleotide-based compounds of the invention are synthesized by a linear synthesis approach (see FIG. 4A).

An alternative mode of synthesis is “parallel synthesis”, in which synthesis proceeds outward from a central linker moiety (see FIG. 4). A solid support attached linker can be used for parallel synthesis, as is described in U.S. Pat. No. 5,912,332. Alternatively, a universal solid support (such as phosphate attached controlled pore glass) support can be used.

Parallel synthesis of the oligonucleotide-based compounds of the invention has several advantages over linear synthesis: (1) parallel synthesis permits the incorporation of identical monomeric units; (2) unlike in linear synthesis, both (or all) the monomeric units are synthesized at the same time, thereby the number of synthetic steps and the time required for the synthesis is the same as that of a monomeric unit; and (3) the reduction in synthetic steps improves purity and yield of the final immune modulatory oligoribonucleotide product.

At the end of the synthesis by either linear synthesis or parallel synthesis protocols, the oligonucleotide-based compounds of the invention may conveniently be deprotected with concentrated ammonia solution or as recommended by the phosphoramidite supplier, if a modified nucleoside is incorporated. The product oligonucleotide-based compounds is preferably purified by reversed phase HPLC, detritylated, desalted and dialyzed.

A non-limiting list of the oligonucleotide-based compounds of the invention are shown in SEQ ID NO. 1 through SEQ ID NO. 175 in Table 3 below. As shown in Table 3, the oligonucleotide-based compounds have phosphorothioate (PS) linkages, but may also include phosphodiester (o) linkages. Those skilled in the art will recognize, however, that other linkages, based on phosphodiester or non-phosphodiester moieties may be included.

TABLE 3 SEQ ID DNA/ Exemplary Sequences of NO./ mRNA RNA the Invention and AS# Target (species) Control Oligonucleotides Structure 1/ TLR9 DNA (h) 5′-ACAGACTTCAGGAACAGCCA-3′ 5′-(SEQ ID NO. 1)-3′ AS1 (Control) 2/ TLR9 DNA (h) 3′-ACCGACAAGGACTTCAGACA-X- 3′-(SEQ ID NO. 2)-5′-X- AS2 ACAGACTTCAGGAACAGCCA-3′ 5′-(SEQ ID NO. 2)-3′ 3/ TLR9 DNA (h) 5′-ACAGACTTCAGGAACAGCCA-X- 5′-(SEQ ID NO. 3)-3′-X- AS3 ACAGACTTCAGGAACAGCCA-3′ 3′-(SEQ ID NO. 3)-5′ (Control) 4/ TLR9 RNA (h) 5′-ACAGACUUCAGGAACAGCCA-3′ 5′-(SEQ ID NO. 4)-3′ AS4 (Control) 5/ TLR9 RNA (m/h) 3′-ACCGACAAGGACUUCAGACA-X- 3′-(SEQ ID NO. 5)-5′-X- AS5 ACAGACUUCAGGAACAGCCA-3′ 5′-(SEQ ID NO. 5)-3′ 6/ TLR9 DNA (m/h) 3′-ACCGACAAGGACTTCAGACA-X- 3′-(SEQ ID NO. 6)-5′-X- AS6 ACAGACTTCAGGAACAGCCA-3′ 5′-(SEQ ID NO. 6)-3′ 7/ TLR9 DNA (m/h) 3′-ACCGACAAGGACTTCAGACA-X- 3′-(SEQ ID NO. 7)-5′-X- AS7 ACAGACTTCAGGAACAGCCA-3′ 5′-(SEQ ID NO. 7)-3′ 8/ TLR9 DNA (m/h) 3′-AoCCoGACAAGGACTTCAoGAoCAo- 3′-(SEQ ID NO. 8)-5′-X- AS8 X-oACoAGoACTTCAGGAACAGoCCoA-3′ 5′-(SEQ ID NO. 8)-3′ 9/ TLR9 DNA (m/h) 3′-ACCGACAAGGACTTCAGACA-X3- 3′-(SEQ ID NO. 9)-5′-X3- AS9 ACAGACTTCAGGAACAGCCA-3′ 5′-(SEQ ID NO. 9)-3′ 10/ TLR9 DNA (m/h) 3′-ACCGACAAGGACTTCAGACA-X1- 3′-(SEQ ID NO. 10)-5′- AS10 ACAGACTTCAGGAACAGCCA-3′ X1-5′-(SEQ ID NO. 10)-3′ 11/ TLR9 DNA (m/h) 3′-ACCGACAAGGACTTCAGACA-Z- 3′-(SEQ ID NO. 11)-5′-Z- AS11 ACAGACTTCAGGAACAGCCA-3′ 5′-(SEQ ID NO. 11)-3′ 12/ TLR9 DNA (m/h) 3′-ACCGACAAGGACTTCAGACA-M- 3′-(SEQ ID NO. 12)-5′-M- AS12 ACAGACTTCAGGAACAGCCA-3′ 5′-(SEQ ID NO. 12)-3′ 13/ TLR9 DNA (m/h) 3′-ACCGACAAGGACTTCAGACA-L- 3′-(SEQ ID NO. 13)-5′-L- AS13 ACAGACTTCAGGAACAGCCA-3′ 5′-(SEQ ID NO. 13)-3′ 14/ TLR9 DNA (m/h) 3′-ACCGACAAGGACTUCAGACA-X- 3′-(SEQ ID NO. 14)-5′-X- AS14 ACAGACUTCAGGAACAGCCA-3′ 5′-(SEQ ID NO. 14)-3′ 15/ TLR9 DNA (m/h) 3′-ACCGACAAGGACTTCAGACA-X- 3′-(SEQ ID NO. 15)-5′-X- AS15 ACAGACTTCAGGAACAGCCA-3′ 5′-(SEQ ID NO. 15)-3′ 16/ TLR9 DNA (m/h) 3′-ACCGACAAGGACUTCAGACA-X- 3′-(SEQ ID NO. 16)-5′-X- AS16 ACAGACTUCAGGAACAGCCA-3′ 5′-(SEQ ID NO. 16)-3′ 17/ TLR9 RNA (m/h) 3′-AGGACUUCAGACA-X- 3′-(SEQ ID NO. 17)-5′-X- AS17 ACAGACUUCAGGA-3′ 5′-(SEQ ID NO. 17)-3′ 18/ TLR9 RNA (m/h) 3′-CAAGGACUUCAGACA-X- 3′-(SEQ ID NO. 18)-5′-X- AS18 ACAGACUUCAGGAAC-3′ 5′-(SEQ ID NO. 18)-3′ 19/ TLR9 RNA (h) 3′-ACGCCGUAGAGUUGGAGUUC-X- 3′-(SEQ ID NO. 19)-5′-X- AS19 CUUGAGGUUGAGAUGCCGCA-3′ 5′-(SEQ ID NO. 19)-3′ 20/ TLR7 DNA (m) 3′-CCTGACGTGTCTGTTCGTAA-X- 3′-(SEQ ID NO. 20)-5′-X- AS20 AATGCTTGTCTGTGCAGTCC-3′ 5′-(SEQ ID NO. 20)-3′ 21/ TLR7 RNA (m) 3′-CCUGACGUGUCUGUUCGUAA-X- 3′-(SEQ ID NO. 21)-5′-X- AS21 AAUGCUUGUCUGUGCAGUCC-3′ 5′-(SEQ ID NO. 21)-3′ 22/ TLR7 RNA (m) 3′-UCGUGUGUUUCCAGUUUCA-X- 3′-(SEQ ID NO. 22)-5′-X- AS22 ACUUUGACCUUUGUGUGCU-3′ 5′-(SEQ ID NO. 22)-3′ 23/ TLR7 RNA (h) 3′-UUGUAGUUGUUUGAGGUCC-X- 3′-(SEQ ID NO. 23)-5′-X- AS23 CCUGGAGUUUGUUGAUGUU-3′ 5′-(SEQ ID NO. 23)-3′ 24/ MyD88 DNA (m) 3′-GTCCGACGATCTCGACGACC-X- 3′-(SEQ ID NO. 24)-5′-X- AS24 CCAGCAGCTCTAGCAGCCTG-3′ 5′-(SEQ ID NO. 24)-3′ 25/ MyD88 RNA (m) 3′-GUCCGACGAUCUCGACGACC-X- 3′-(SEQ ID NO. 25)-5′-X- AS25 CCAGCAGCUCUAGCAGCCUG-3′ 5′-(SEQ ID NO. 25)-3′ 26/ TLR7 DNA (m) 5′-AATGCTTGTCTGTGCAGTCC-3′ 5′-(SEQ ID NO. 26)-3′ AS26 (Control) 27/ TLR7 DNA (m) 3′-CCTGACGTGTCTGTTCGTAA-X- 3′-(SEQ ID NO. 27)-5′-X- AS27 AATGCTTGTCTGTGCAGTCC-3′ 5′-(SEQ ID NO. 27)-3′ 28/ TLR7 RNA(m/h) 3′-CCUGACGUGUCUGUUCGUAA-5′ 3′-(SEQ ID NO. 28)-5′ AS28 (Control) 29/ TLR7 RNA (m/h) 5′- 5′-(SEQ ID NO. 29)-3′ AS29 CUGUCoAoAoAoUoGoCoUoUoGoUoCoUo GoUoGoCoAoGoUoCoCo ACGAU-3′ (Control) 30/ TLR9 DNA (m/h) 3′-CCGACAAGGACTTCAGACA-X- 3′-(SEQ ID NO. 30)-5′-X- AS30 ACAGACTTCAGGAACAGCC-3′ 5′-(SEQ ID NO. 30)-3′ 31/ TLR9 DNA (m/h) 5′-ACAGACTTCAGGAACAGCC-X- 5′-(SEQ ID NO. 31)-3′-X- AS31 CCGACAAGGACTTCAGACA-5′ (Control) 3′-(SEQ ID NO. 31)-5′ 32/ TLR9 DNA (m/h) 5′-ACAGACTTCAGGAACAGCC-3′ 5′-(SEQ ID NO. 32)-3′ AS32 (Control) 33/ TLR7 DNA (m/h) 3′-CTGACGTGTCTGTTCGTAA-X- 3′-(SEQ ID NO. 33)-5′-X- AS33 AATGCTTGTCTGTGCAGTC-3′ 5′-(SEQ ID NO. 33)-3′ 34/ TLR7 DNA (m/h) 5′-AATGCTTGTCTGTGCAGTC-X- 5′-(SEQ ID NO. 34)-3′-X- AS34 CTGACGTGTCTGTTCGTAA-5′ (Control) 3′-(SEQ ID NO. 34)-5′ 35/ TLR7 DNA (m/h) 5′-AATGCTTGTCTGTGCAGTCC-3′ 5′-(SEQ ID NO. 35)-3′ AS35 (Control) 36/ MyD88 DNA (h) 3′-CGTTGACCTCTGTGTTCGC-X- 3′-(SEQ ID NO. 36)-5′-X- AS36 CGCTTGTGTCTCCAGTTGC-3′ 5′-(SEQ ID NO. 36)-3′ 37/ MyD88 DNA (h) 5′-CGCTTGTGTCTCCAGTTGC-X- 5′-(SEQ ID NO. 37)-3′-X- AS37 CGTTGACCTCTGTGTTCGC-5′ (Control) 3′-(SEQ ID NO. 37)-5′ 38/ MyD88 DNA (h) 5′-CGCTTGTGTCTCCAGTTGC-3′ 5′-(SEQ ID NO. 38)-3′ AS38 (Control) 39/ VEGF DNA (h) 3′- GAAAGACGACAGAACCCAC-X- 3′-(SEQ ID NO. 39)-5′-X- AS39 CACCCAAGACAGCAGAAAG-3′ 5′-(SEQ ID NO. 39)-3′ 40/ VEGF DNA (h) 5′-CACCCAAGACAGCAGAAAG-X- 5′-(SEQ ID NO. 40)-3′-X- AS40 GAAAGACGACAGAACCCAC-5′ (Control) 3′-(SEQ ID NO. 40)-5′ 41/ VEGF DNA (h) 5′-CACCCAAGACAGCAGAAAG-3′ 5′-(SEQ ID NO. 41)-3′ AS41 (Control) 42/ TLR9 DNA (m/h) 3′-CAAGGACTTCAGACA-X- 3′-(SEQ ID NO. 42)-5′-X- AS42 ACAGACTTCAGGAAC-3′ 5′-(SEQ ID NO. 42)-3′ 43/ TLR9 DNA (m/h) 3′-GACAAGGACTTCAGACA-X- 3′-(SEQ ID NO. 43)-5′-X- AS43 ACAGACTTCAGGAACAG-3′ 5′-(SEQ ID NO. 43)-3′ 44/ TLR9 DNA (m/h) 3′-CCGACAAGGACTTCAGACA-X- 3′-(SEQ ID NO. 44)-5′-X- AS44 ACAGACTTCAGGAACAGCC-3′ 5′-(SEQ ID NO. 44)-3′ 45/ TLR9 DNA (m/h) 3′-AACCGACAAGGACTTCAGACA-X- 3′-(SEQ ID NO. 45)-5′-X- AS45 ACAGACTTCAGGAACAGCCAA-3′ 5′-(SEQ ID NO. 45)-3′ 46/ TLR9 DNA (m/h) 3′-TTAACCGACAAGGACTTCAGACA-X- 3′-(SEQ ID NO. 46)-5′-X- AS46 ACAGACTTCAGGAACAGCCAATT-3′ 5′-(SEQ ID NO. 46)-3′ 47/ TLR9 DNA (m/h) 3′- 3′-(SEQ ID NO. 47)-5′-X- AS47 CGTTAACCGACAAGGACTTCAGACA-X- 5′-(SEQ ID NO. 47)-3′ ACAGACTTCAGGAACAGCCAATTGC-3′ 48/ TLR9 DNA (m/h) 3′- 3′-(SEQ ID NO. 48)-5′-X- AS48 GACGTTAACCGACAAGGACTTCAGACA-X- 5′-(SEQ ID NO. 48)-3′ ACAGACTTCAGGAACAGCCAATTGCAG-3′ 49/ TLR9 DNA (h) 3′-GACCGACAAGGACUUCAGACA-X- 3′-(SEQ ID NO. 49)-5′-X- AS49 ACAGACUUCAGGAACAGCCAG-3′ 5′-(SEQ ID NO. 49)-3′ 50/ TLR9 DNA (h) 3′-TTGACCGACAAGGACUUCAGACA-X- 3′-(SEQ ID NO. 50)-5′-X- AS50 ACAGACUUCAGGAACAGCCAGTT-3′ 5′-(SEQ ID NO. 50)-3′ 51/ TLR9 DNA (m/h) 3′- 3′-(SEQ ID NO. 51)-5′-X- AS51 CoCoGoAoCoAoAoGoGoAoCoToToCoAoG 5′-(SEQ ID NO. 51)-3′ oAoCoAo-X- oAoCoAoGoAoCoToToCoAoGoGoAoAoCo AoGoCoC-3′ 52/ TLR9 DNA (m/h) 5′-C-3′-3′-CCGACAAGGACTTCAGACA- 3′-(SEQ ID NO. 52)-5′-X- AS52 X-ACAGACTTCAGGAACAGCC-3′-3′-C- 5′-(SEQ ID NO. 52)-3′ 5′ 53/ TLR9 DNA (m/h) 5′-GCC-3′-3′- 3′-(SEQ ID NO. 53)-5′-X- AS53 CCGACAAGGACTTCAGACA-X- 5′-(SEQ ID NO. 53)-3′ ACAGACTTCAGGAACAGCC-3′-3′-CCG- 5′ 54/ TLR9 DNA (m/h) 5′-CAGCC-3′-3′- 3′-(SEQ ID NO. 54)-5′-X- AS54 CCGACAAGGACTTCAGACA-X- 5′-(SEQ ID NO. 54)-3′ ACAGACTTCAGGAACAGCC3′-3′- CCGAC-5′ 55/ TLR9 DNA (m/h) 3′-CCGACAAGGACTTCAGACA-X- 3′-(SEQ ID NO. 55)-5′-X- AS55 ACAGACTTCAGGAACAGCC-3′ 5′-(SEQ ID NO. 55)-3′ 56/ TLR9 DNA (m/h) 3′-CCGACAAGGACTTCAGACA-X- 3′-(SEQ ID NO. 56)-5′-X- AS56 ACAGACTTCAGGAACAGCC-3′ 5′-(SEQ ID NO. 56)-3′ 57/ TLR9 DNA (m/h) 3′-CCGACAAGGACTTCAGACA- 3′-(SEQ ID NO. 57)-5′-X- AS57 ACAGACTTCAGGAACAGCC-3′ 5′-(SEQ ID NO. 57)-3′ 58/ TLR9 DNA (m/h) 3′-CCGACAAGGACTTCAGACA-Y- 3′-(SEQ ID NO. 58)-5′-X- AS58 ACAGACTTC-3′ 5′-(SEQ ID NO. 58)-3′ 59/ TLR9 DNA (m/h) 3′-CTTCAGACA-X-ACAGACTTC-3′ 3′-(SEQ ID NO. 59)-5′-X- AS59 5′-(SEQ ID NO. 59)-3′ 60/ TLR9 DNA (m/h) 3′-CCGACAAGGACTTCAGACA-X- 3′-(SEQ ID NO. 60)-5′-X- AS60 ACAGACTTCAGGAACAGCC-3′ 5′-(SEQ ID NO. 60)-3′ 61/ TLR9 DNA (m/h) 3′-TTGACCGACAAGGACTTCAGACA-X- 3′-(SEQ ID NO. 61)-5′-X- AS61 ACAGACTTCAGGAACAGCCAGTT-3′ 5′-(SEQ ID NO. 61)-3′ 62/ TLR9 DNA (m/h) 3′-CCGACAAGGACTTCAGACA-X5- 3′-(SEQ ID NO. 62)-5′-X- AS62 ACAGACTTCAGGAACAGCC-3′ 5′-(SEQ ID NO. 62)-3′ 63/ TLR7 DNA (m/h) 3′-GACGTGTCTGTTCGTAA-X- 3′-(SEQ ID NO. 63)-5′-X- AS63 AATGCTTGTCTGTGCAG-3′ 5′-(SEQ ID NO. 63)-3′ 64/ TLR7 DNA (m/h) 3′-CTGACGTGTCTGTTCGTAA-X- 3′-(SEQ ID NO. 64)-5′-X- AS64 AATGCTTGTCTGTGCAGTC-3′ 5′-(SEQ ID NO. 64)-3′ 65/ TLR7 DNA (m/h) 3′-ACCTGACGTGTCTGTTCGTAA-X- 3′-(SEQ ID NO. 65)-5′-X- AS65 AATGCTTGTCTGTGCAGTCCA-3′ 5′-(SEQ ID NO. 65)-3′ 66/ MyD88 DNA (m) 3′-ACGATCTCGACGACC-X- 3′-(SEQ ID NO. 66)-5′-X- AS66 CCAGCAGCTCTAGCA-3′ 5′-(SEQ ID NO. 66)-3′ 67/ MyD88 DNA (m) 3′-CGACGATCTCGACGACC-X- 3′-(SEQ ID NO. 67)-5′-X- AS67 CCAGCAGCTCTAGCAGC-3′ 5′-(SEQ ID NO. 67)-3′ 68/ MyD88 DNA (m) 3′-TCCGACGATCTCGACGACC-X- 3′-(SEQ ID NO. 68)-5′-X- AS68 CCAGCAGCTCTAGCAGCCT-3′ 5′-(SEQ ID NO. 68)-3′ 69/ MyD88 DNA (m) 3′-CGTCCGACGATCTCGACGACC-X- 3′-(SEQ ID NO. 69)-5′-X- AS69 CCAGCAGCTCTAGCAGCCTGC-3′ 5′-(SEQ ID NO. 69)-3′ 70/ MyD88 DNA (m) 3′-GCCGTCCGACGATCTCGACGACC-X- 3′-(SEQ ID NO. 70)-5′-X- AS70 CCAGCAGCTCTAGCAGCCTGCCG-3′ 5′-(SEQ ID NO. 70)-3′ 71/ MyD88 DNA (m) 3′-CAGCCGTCCGACGATCTCGACGACC- 3′-(SEQ ID NO. 71)-5′-X- AS71 X-CCAGCAGCTCTAGCAGCCTGCCGAC-3′ 5′-(SEQ ID NO. 71)-3′ 72/ MyD88 DNA (h) 3′-GACCTCTGTGTTCGC-X- 3′-(SEQ ID NO. 72)-5′-X- AS72 CGCTTGTGTCTCCAG-3′ 5′-(SEQ ID NO. 72)-3′ 73/ MyD88 DNA (h) 3′-TTGACCTCTGTGTTCGC-X- 3′-(SEQ ID NO. 73)-5′-X- AS73 CGCTTGTGTCTCCAGTT-3′ 5′-(SEQ ID NO. 73)-3′ 74/ MyD88 DNA (h) 3′-CGTTGACCTCTGTGTTCGC-X- 3′-(SEQ ID NO. 74)-5′-X- AS74 CGCTTGTGTCTCCAGTTGC-3′ 5′-(SEQ ID NO. 74)-3′ 75/ MyD88 DNA (h) 3′-GCCGTTGACCTCTGTGTTCGC-X- 3′-(SEQ ID NO. 75)-5′-X- AS75 CGCTTGTGTCTCCAGTTGCCG-3′ 5′-(SEQ ID NO. 75)-3′ 76/ MyD88 DNA (h) 3′-AGGCCGTTGACCTCTGTGTTCGC-X- 3′-(SEQ ID NO. 76)-5′-X- AS76 CGCTTGTGTCTCCAGTTGCCGGA-3′ 5′-(SEQ ID NO. 76)-3′ 77/ MyD88 DNA (h) 3′-CTAGGCCGTTGACCTCTGTGTTCGC- 3′-(SEQ ID NO. 77)-5′-X- AS77 X-CGCTTGTGTCTCCAGTTGCCGGATC-3′ 5′-(SEQ ID NO. 77)-3′ 78/ MyD88 DNA (m) 3′-UCCGACGATCTCGACGACC-X- 3′-(SEQ ID NO. 78)-5′-X- AS78 CCAGCAGCTCTAGCAGCCU-3′ 5′-(SEQ ID NO. 78)-3′ 79/ MyD88 DNA (h) 3′-CGUUGACCTCTGTGTUCGC-X- 3′-(SEQ ID NO. 79)-5′-X- AS79 CGCUTGTGTCTCCAGUUGC-3′ 5′-(SEQ ID NO. 79)-3′ 80/ MyD88 DNA (h) 3′-CGTTGACCTCTGTGTTCGC-Z- 3′-(SEQ ID NO. 80)-5′-X- AS80 CGCTTGTGTCTCCAGTTGC-3′ 5′-(SEQ ID NO. 80)-3′ 81/ MyD88 DNA (h) (3′-CGTTGACCTCTGTGTTCGC)₂-Z-Z-Z- 3′-(SEQ ID NO. 81)-5′-X- AS81 (CGCTTGTGTCTCCAGTTGC-3′)₂ 5′-(SEQ ID NO. 81)-3′ 82/ TLR3 DNA (m) 3′-CTTGGAGGTTCTTGACG-X- 3′-(SEQ ID NO. 82)-5′-X- AS82 GCAGTTCTTGGAGGTTC-3′ 5′-(SEQ ID NO. 82)-3′ 83/ TLR3 DNA (m) 3′-CTCTTGGAGGTTCTTGACG-X- 3′-(SEQ ID NO. 83)-5′-X- AS83 GCAGTTCTTGGAGGTTCTC-3′ 5′-(SEQ ID NO. 83)-3′ 84/ TLR3 DNA (m) 3′-ACCTCTTGGAGGTTCTTGACG-X- 3′-(SEQ ID NO. 84)-5′-X- AS84 GCAGTTCTTGGAGGTTCTCCA-3′ 5′-(SEQ ID NO. 84)-3′ 85/ TLR3 DNA (h) 3′-CGTGGAATTGTACCTTC-X- 3′-(SEQ ID NO. 85)-5′-X- AS85 CTTCCATGTTAAGGTGC-3′ 5′-(SEQ ID NO. 85)-3′ 86/ TLR3 DNA (h) 3′-CTCGTGGAATTGTACCTTC-X- 3′-(SEQ ID NO. 86)-5′-X- AS86 CTTCCATGTTAAGGTGCTC-3′ 5′-(SEQ ID NO. 86)-3′ 87/ TLR3 DNA (h) 3′-ACCTCGTGGAATTGTACCTTC-X- 3′-(SEQ ID NO. 87)-5′-X- AS87 CTTCCATGTTAAGGTGCTCCA-3′ 5′-(SEQ ID NO. 87)-3′ 88/ VEGF DNA (h) 3′-GAAAGACGACAGAACCCAC-X- 3′-(SEQ ID NO. 88)-5′-X- AS88 CACCCAAGACAGCAGAAAG-3′ 5′-(SEQ ID NO. 88)-3′ 89/ Mdm2 DNA (h) 3′-CACTCTTGTCCACAG-X- 3′-(SEQ ID NO. 89)-5′-X- AS89 GACACCTGTTCTCAC-3′ 5′-(SEQ ID NO. 89)-3′ 90/ Mdm2 DNA (h) 3′-CTCACTCTTGTCCACAG-X- 3′-(SEQ ID NO. 90)-5′-X- AS90 GACACCTGTTCTCACTC-3′ 5′-(SEQ ID NO. 90)-3′ 91/ Mdm2 DNA (h) 3′-CACTCACTCTTGTCCACAG-X- 3′-(SEQ ID NO. 91)-5′-X- AS91 GACACCTGTTCTCACTCAC-3′ 5′-(SEQ ID NO. 91)-3′ 92/ Mdm2 DNA (h) 3′-GACACTCACTCTTGTCCACAG-X- 3′-(SEQ ID NO. 92)-5′-X- AS92 GACACCTGTTCTCACTCACAG-3′ 5′-(SEQ ID NO. 92)-3′ 93/ Mdm2 DNA (h) 3′-TAGACACTCACTCTTGTCCACAG-X- 3′-(SEQ ID NO. 93)-5′-X- AS93 GACACCTGTTCTCACTCACAGAT-3′ 5′-(SEQ ID NO. 93)-3′ 94/ Mdm2 DNA (h) 3′-CACTCACTCTTGTCCACAG-Y- 3′-(SEQ ID NO. 94)-5′-X- AS94 GACACCTGT-3′ 5′-(SEQ ID NO. 94)-3′ 95/ Mdm2 DNA (h) 3′-TGTCCACAG-X-GACACCTGT-3′ 3′-(SEQ ID NO. 95)-5′-X- AS95 5′-(SEQ ID NO. 95)-3′ 96/ BCL2 DNA (h) 3′-CCTCTATCACTACTTCATG-X- 3′-(SEQ ID NO. 96)-5′-X- AS96 GTACTTCATCACTATCTCC-3′ 5′-(SEQ ID NO. 96)-3′ 97/ Survivin DNA (h) 3′-CCTGTCTCTTTCTCGGTTC-X- 3′-(SEQ ID NO. 97)-5′-X- AS97 CTTGGCTCTTTCTCTGTCC-3′ 5′-(SEQ ID NO. 97)-3′ 98/ EGFR DNA (h) 3′-GTTCGACACTGTCTAGTAT-X- 3′-(SEQ ID NO. 98)-5′-X- AS98 TATGATCTGTCACAGCTTG-3′ 5′-(SEQ ID NO. 98)-3′ 99/ EGFR DNA (h) 3′-CTTTCCCTCCTTTGGATCG-X- 3′-(SEQ ID NO. 99)-5′-X- AS99 GCTAGGTTTCCTCCCTTTC-3′ 5′-(SEQ ID NO. 99)-3′ 100/ PCSK9 DNA (h) 3′-CTCCGTCTCTGACTAGGTG-X- 3′-(SEQ ID NO. 100)-5′- AS100 GTGGATCAGTCTCTGCCTC-3′ X-5′-(SEQ ID NO. 100)-3′ 101/ PCSK9 DNA (h) 3′-CGTCGGACCACCTCCACAT-Y- 3′-(SEQ ID NO. 101)-5′- AS101 TACACCTCC-3′ X-5′-(SEQ ID NO. 101)-3′ 102/ PCSK9 DNA (h) 3′-CTCCGTCTCTGACTAGGTG-Y- 3′-(SEQ ID NO. 102)-5′- AS102 GTGGATCAG-3′ X-5′-(SEQ ID NO. 102)-3′ 103/ PCSK9 DNA (h) 3′-AGACCTTACGTTTCAGTTC-Y- 3′-(SEQ ID NO. 103)-5′- AS103 CTTGACTTT-3′ X-5′-(SEQ ID NO. 103)-3′ 104/ PCSK9 DNA (h) 3′-CCTCCACAT-X-TACACCTCC-3′ 3′-(SEQ ID NO. 104)-5′- AS104 X-5′-(SEQ ID NO. 104)-3′ 105/ PCSK9 DNA (h) 3′-GACTAGGTG-X-GTGGATCAG-3′ 3′-(SEQ ID NO. 105)-5′- AS105 X-5′-(SEQ ID NO. 105)-3′ 106/ PCSK9 DNA (h) 3′-TTTCAGTTC-X-CTTGACTTT-3′ 3′-(SEQ ID NO. 106)-5′- AS106 X-5′-(SEQ ID NO. 106)-3′ 107/ PCSK9 DNA (h) 3′-AGACCTTACGTTTCA-X- 3′-(SEQ ID NO. 107)-5′- AS107 ACTTTGCATTCCAGA-3′ X-5′-(SEQ ID NO. 107)-3′ 108/ PCSK9 DNA (h) 3′-AGACCTTACGTTTCAGT-X- 3′-(SEQ ID NO. 108)-5′- AS108 TGACTTTGCATTCCAGA-3′ X-5′-(SEQ ID NO. 108)-3′ 109/ PCSK9 DNA (h) 3′-AGACCTTACGTTTCAGTTC-X- 3′-(SEQ ID NO. 109)-5′- AS109 CTTGACTTTGCATTCCAGA-3′ X-5′-(SEQ ID NO. 109)-3′ 110/ PCSK9 DNA (h) 3′-AGACCTTACGTTTCAGTTCCT-X- 3′-(SEQ ID NO. 110)-5′- AS110 TCCTTGACTTTGCATTCCAGA-3′ X-5′-(SEQ ID NO. 110)-3′ 111/ PCSK9 DNA (h) 3′-AGACCTTACGTTTCAGTTCCTCG-X- 3′-(SEQ ID NO. 111)-5′- AS111 GCTCCTTGACTTTGCATTCCAGA-3′ X-5′-(SEQ ID NO. 111)-3′ 112/ PCSK9 DNA (h) 3′-AGACCTTACGTTTCAGTTCCTCGTA- 3′-(SEQ ID NO. 112)-5′- AS112 X-ATGCTCCTTGACTTTGCATTCCAGA- X-5′-(SEQ ID NO. 112)-3′ 3′ 113/ PCSK9 DNA (h) 3′-CGTCGGACCACCTCC-X- 3′-(SEQ ID NO. 113)-5′- AS113 CCTCCACCAGGCTGC-3′ X-5′-(SEQ ID NO. 113)-3′ 114/ PCSK9 DNA (h) 3′-CGTCGGACCACCTCCAC-X- 3′-(SEQ ID NO. 114)-5′- AS114 CACCTCCACCAGGCTGC-3′ X-5′-(SEQ ID NO. 114)-3′ 115/ PCSK9 DNA (h) 3′-CGTCGGACCACCTCCACAT-X- 3′-(SEQ ID NO. 115)-5′- AS115 TACACCTCCACCAGGCTGC-3′ X-5′-(SEQ ID NO. 115)-3′ 116/ PCSK9 DNA (h) 3′-CGTCGGACCACCTCCACATAG-X- 3′-(SEQ ID NO. 116)-5′- AS116 GATACACCTCCACCAGGCTGC-3′ X-5′-(SEQ ID NO. 116)-3′ 117/ PCSK9 DNA (h) 3′-CGTCGGACCACCTCCACATAGAG-X- 3′-(SEQ ID NO. 117)-5′- AS117 GAGATACACCTCCACCAGGCTGC-3′ X-5′-(SEQ ID NO. 117)-3′ 118/ PCSK9 DNA (h) 3′- 3′-(SEQ ID NO. 118)-5′- AS118 CGTCGGACCACCTCCACATAGAGGA-X- X-5′-(SEQ ID NO. 118)-3′ AGGAGATACACCTCCACCAGGCTGC-3′ 119/ PCSK9 DNA (m) 3′-CCAGGAAGTCTCGTCCAGT-X- 3′-(SEQ ID NO. 119)-5′- AS119 TGACCTGCTCTGAAGGACC-3′ X-5′-(SEQ ID NO. 119)-3′ 120/ TLR9 RNA (m/h) 3′-GACAAGGACUUCAGACA-X- 3′-(SEQ ID NO. 120)-5′- AS 120 ACAGACUUCAGGAACAG-3′ X-5′-(SEQ ID NO. 120)-3′ 121/ TLR9 RNA (m/h) 3′-CCGACAAGGACUUCAGACA-X- 3′-(SEQ ID NO. 121)-5′- AS121 ACAGACUUCAGGAACAGCC-3′ X-5′-(SEQ ID NO. 121)-3′ 122/ TLR9 RNA (m) 3′-AACCGACAAGGACUUCAGACA-X- 3′-(SEQ ID NO. 122)-5′- AS122 ACAGACUUCAGGAACAGCCAA-3′ X-5′-(SEQ ID NO. 122)-3′ 123/ TLR9 RNA (m) 3′-UUAACCGACAAGGACUUCAGACA- 3′-(SEQ ID NO. 123)-5′- AS123 X-ACAGACUUCAGGAACAGCCAAUU-3′ X-5′-(SEQ ID NO. 123)-3′ 124/ TLR9 RNA (m) 3′-CGUUAACCGACAAGGACUUCAGACA- 3′-(SEQ ID NO. 124)-5′- AS124 X-ACAGACUUCAGGAACAGCCAAUUGC-3′ X-5′-(SEQ ID NO. 124)-3′ 125/ TLR9 RNA (m) 3′- 3′-(SEQ ID NO. 125)-5′- AS125 GACGUUAACCGACAAGGACUUCAGACA-X- X-5′-(SEQ ID NO. 125)-3′ ACAGACUUCAGGAACAGCCAAUUGCAG-3′ 126/ TLR9 RNA (h) 3′-GACCGACAAGGACUUCAGACA-X- 3′-(SEQ ID NO. 126)-5′- AS126 ACAGACUUCAGGAACAGCCAG-3′ X-5′-(SEQ ID NO. 126)-3′ 127/ TLR9 RNA (h) 3′-UUGACCGACAAGGACUUCAGACA- 3′-(SEQ ID NO. 127)-5′- AS127 X-ACAGACUUCAGGAACAGCCAGUU-3′ X-5′-(SEQ ID NO. 127)-3′ 128/ TLR9 RNA (h) 3′- 3′-(SEQ ID NO. 128)-5′- AS128 CGUUGACCGACAAGGACUUCAGACA-X- X-5′-(SEQ ID NO. 128)-3′ ACAGACUUCAGGAACAGCCAGUUGC-3′ 129/ TLR9 RNA (m/h) 3′-ACCGACAAGGACUUCAGACA-Y-AC-3′ 3′-(SEQ ID NO. 129)-5′- AS129 X-5′-(SEQ ID NO. 129)-3′ 130/ TLR9 RNA (m/h) 3′-ACCGACAAGGACUUCAGACA-Y- 3′-(SEQ ID NO. 130)-5′- AS130 ACAG-3′ X-5′-(SEQ ID NO. 130)-3′ 131/ TLR9 RNA (m/h) 3′-ACCGACAAGGACUUCAGACA-Y- 3′-(SEQ ID NO. 131)-5′- AS131 ACAGAC-3′ X-5′-(SEQ ID NO. 131)-3′ 132/ TLR9 RNA (m/h) 3′-ACCGACAAGGACUUCAGACA-X3- 3′-(SEQ ID NO. 132)-5′- AS132 ACAGACUUCAGGAACAGCCA-3′ X-5′-(SEQ ID NO. 132)-3′ 133/ TLR9 RNA (m/h) 3′-ACCGACAAGGACUUCAGACA-X1- 3′-(SEQ ID NO. 133)-5′- AS133 ACAGACUUCAGGAACAGCCA′-3 X-5′-(SEQ ID NO. 133)-3′ 134/ TLR9 RNA (m/h) 3′-ACCGACAAGGACUUCAGACA-Z- 3′-(SEQ ID NO. 134)-5′- AS134 ACAGACUUCAGGAACAGCCA′-3 X-5′-(SEQ ID NO. 134)-3′ 135/ TLR9 RNA (m/h) 3′-ACCGACAAGGACUUCAGACA-M- 3′-(SEQ ID NO. 135)-5′- AS135 ACAGACUUCAGGAACAGCCA-3′ X-5′-(SEQ ID NO. 135)-3′ 136/ TLR9 RNA (m/h) 3′-ACCGACAAGGACUUCAGACA-L- 3′-(SEQ ID NO. 136)-5′- AS136 ACAGACUUCAGGAACAGCCA-3′ X-5′-(SEQ ID NO. 136)-3′ 137/ TLR9 RNA (m/h) 3′-ACCGACAAGGACUUCAGACA-X- 3′-(SEQ ID NO. 137)-5′- AS137 ACAGACUUCAGGAACAGCCA-3′ X-5′-(SEQ ID NO. 137)-3′ 138/ TLR9 RNA (m/h) 3′-ACCGACAAGGACUUCAGACA-X- 3′-(SEQ ID NO. 138)-5′- AS138 ACAGACUUCAGGAACAGCCA-3′ X-5′-(SEQ ID NO. 138)-3′ 139/ TLR9 RNA (m) 3′-AACCGACAAGGACUUCAGACA-X- 3′-(SEQ ID NO. 139)-5′- AS139 ACAGACUUCAGGAACAGCCAA-3′ X-5′-(SEQ ID NO. 139)-3′ 140/ TLR9 RNA (m) 3′-AACCGACAAGGACUUCAGACA-X- 3′-(SEQ ID NO. 140)-5′- AS140 ACAGACUUCAGGAACAGCCAA-3′ X-5′-(SEQ ID NO. 140)-3′ 141/ TLR9 RNA (m) 3′-AACCGACAAGGACUUCAGACA-X- 3′-(SEQ ID NO. 141)-5′- AS141 ACAGACUUCAGGAACAGCCAA-3′ X-5′-(SEQ ID NO. 141)-3′ 142/ TLR9 RNA (m) 3′-AACCGACAAGGACUUCAGACA-X- 3′-(SEQ ID NO. 142)-5′- AS142 ACAGACUUCAGGAACAGCCAA-3′ X-5′-(SEQ ID NO. 142)-3′ 143/ TLR9/ RNA/ 3′-ACCGACAAGGACUUCAGACA-Y- 3′-(SEQ ID NO. 132)-5′- AS143 TLR7 DNA (m/h) d(AATGCTTGTCTGTGCAGTCC)-3′ X-5′-(SEQ ID NO. 35)-3′ 144/ MyD88 RNA (m) 3′-ACGAUCUCGACGACC-X- 3′-(SEQ ID NO. 144)-5′- AS144 CCAGCAGCUCUAGCA-3′ X-5′-(SEQ ID NO. 144)-3′ 145/ MyD88 RNA (m) 3′-CGACGAUCUCGACGACC-X- 3′-(SEQ ID NO. 145)-5′- AS145 CCAGCAGCUCUAGCAGC-3′ X-5′-(SEQ ID NO. 145)-3′ 146/ MyD88 RNA (m) 3′-UCCGACGAUCUCGACGACC-X- 3′-(SEQ ID NO. 146)-5′- AS146 CCAGCAGCUCUAGCAGCCU-3′ X-5′-(SEQ ID NO. 146)-3′ 147/ MyD88 RNA (m) 3′-CGUCCGACGAUCUCGACGACC-X- 3′-(SEQ ID NO. 147)-5′- AS147 CCAGCAGCUCUAGCAGCCUGC-3′ X-5′-(SEQ ID NO. 147)-3′ 148/ MyD88 RNA (m) 3′-GCCGUCCGACGAUCUCGACGACC-X- 3′-(SEQ ID NO. 148)-5′- AS148 CCAGCAGCUCUAGCAGCCUGCCG-3′ X-5′-(SEQ ID NO. 148)-3′ 149/ MyD88 RNA (m) 3′-CAGCCGUCCGACGAUCUCGACGACC- 3′-(SEQ ID NO. 149)-5′- AS149 X-CCAGCAGCUCUAGCAGCCUGCCGAC-3′ X-5′-(SEQ ID NO. 149)-3′ 150/ MyD88 RNA (h) 3′-GACCUCUGUGUUCGC-X- 3′-(SEQ ID NO. 150)-5′- AS150 CGCUUGUGUCUCCAG-3′ X-5′-(SEQ ID NO. 150)-3′ 151/ MyD88 RNA (h) 3′-UUGACCUCUGUGUUCGC-X- 3′-(SEQ ID NO. 151)-5′- AS151 CGCUUGUGUCUCCAGUU-3′ X-5′-(SEQ ID NO. 151)-3′ 152/ MyD88 RNA (h) 3′-CGUUGACCUCUGUGUUCGC-X- 3′-(SEQ ID NO. 152)-5′- AS152 CGCUUGUGUCUCCAGUUGC-3′ X-5′-(SEQ ID NO. 152)-3′ 153/ MyD88 RNA (h) 3′-GCCGUUGACCUCUGUGUUCGC-X- 3′-(SEQ ID NO. 153)-5′- AS153 CGCUUGUGUCUCCAGUUGCCG-3′ X-5′-(SEQ ID NO. 153)-3′ 154/ MyD88 RNA (h) 3′-AGGCCGUUGACCUCUGUGUUCGC- 3′-(SEQ ID NO. 154)-5′- AS154 X-CGCUUGUGUCUCCAGUUGCCGGA-3′ X-5′-(SEQ ID NO. 154)-3′ 155/ MyD88 RNA (h) 3′-CUAGGCCGUUGACCUCUGUGUUCGC- 3′-(SEQ ID NO. 155)-5′- AS155 X-CGCUUGUGUCUCCAGUUGCCGGAUC-3′ X-5′-(SEQ ID NO. 155)-3′ 156/ TLR7 RNA (m/h) 3′-CGUGUCUGUUCGUAA-X- 3′-(SEQ ID NO. 156)-5′- AS156 AAUGCUUGUCUGUGC-3′ X-5′-(SEQ ID NO. 156)-3′ 157/ TLR7 RNA (m/h) 3′-GACGUGUCUGUUCGUAA-X- 3′-(SEQ ID NO. 157)-5′- AS157 AAUGCUUGUCUGUGCAG-3′ X-5′-(SEQ ID NO. 157)-3′ 158/ TLR7 RNA (m/h) 3′-CUGACGUGUCUGUUCGUAA-X- 3′-(SEQ ID NO. 158)-5′- AS158 AAUGCUUGUCUGUGCAGUC-3′ X-5′-(SEQ ID NO. 158)-3′ 159/ TLR7 RNA (m/h) 3′-ACCUGACGUGUCUGUUCGUAA-X- 3′-(SEQ ID NO. 159)-5′- AS159 AAUGCUUGUCUGUGCAGUCCA-3′ X-5′-(SEQ ID NO. 159)-3′ 160/ TLR7 RNA (m/h) 3′-GCACCUGACGUGUCUGUUCGUAA- 3′-(SEQ ID NO. 160)-5′- AS160 X-AAUGCUUGUCUGUGCAGUCCACG-3′ X-5′-(SEQ ID NO. 160)-3′ 161/ TLR7 RNA (m/h) 3′-UAGCACCUGACGUGUCUGUUCGUAA- 3′-(SEQ ID NO. 161)-5′- AS161 X-AAUGCUUGUCUGUGCAGUCCACGAU-3′ X-5′-(SEQ ID NO. 161)-3′ 162/ TLR7/ RNA/ 3′-CCUGACGUGUCUGUUCGUAA-Y- 3′-(SEQ ID NO. 21)-5′-X- AS162 TLR9 DNA (m/h) d(ACAGACTTCAGGAACAGCCA)-3′ 5′-(SEQ ID NO. 1)-3′ 163/ TLR3 RNA (m) 3′-CUUGGAGGUUCUUGACG-X- 3′-(SEQ ID NO. 163)-5′- AS163 GCAGUUCUUGGAGGUUC-3′ X-5′-(SEQ ID NO. 163)-3′ 164/ TLR3 RNA (m) 3′-CUCUUGGAGGUUCUUGACG-X- 3′-(SEQ ID NO. 164)-5′- AS164 GCAGUUCUUGGAGGUUCUC-3′ X-5′-(SEQ ID NO. 164)-3′ 165/ TLR3 RNA (m) 3′-ACCUCUUGGAGGUUCUUGACG-X- 3′-(SEQ ID NO. 165)-5′- AS165 GCAGUUCUUGGAGGUUCUCCA-3′ X-5′-(SEQ ID NO. 165)-3′ 166/ TLR3 RNA (m) 3′-CAAGUCGUUCGAUAACUCG-X- 3′-(SEQ ID NO. 166)-5′- AS166 GCUCAAUAGCUUGCUGAAC-3′ X-5′-(SEQ ID NO. 166)-3′ 167/ TLR3 RNA (h) 3′-CGUGGAAUUGUACCUUC-X- 3′-(SEQ ID NO. 167)-5′- AS167 CUUCCAUGUUAAGGUGC-3′ X-5′-(SEQ ID NO. 167)-3′ 168/ TLR3 RNA (h) 3′-CUCGUGGAAUUGUACCUUC-X- 3′-(SEQ ID NO. 168)-5′- AS168 CUUCCAUGUUAAGGUGCUC-3′ X-5′-(SEQ ID NO. 168)-3′ 169/ TLR3 RNA (h) 3′-ACCUCGUGGAAUUGUACCUUC-X- 3′-(SEQ ID NO. 169)-5′- AS169 CUUCCAUGUUAAGGUGCUCCA-3′ X-5′-(SEQ ID NO. 169)-3′ 170/ TLR3 RNA (h) 3′-GUUGUUGUUGUAUCGGUUG-X- 3′-(SEQ ID NO. 170)-5′- AS170 GUUGGCUAUGUUGUUGUUG-3′ X-5′-(SEQ ID NO. 170)-3′ 171/ MDM2 RNA (h) 3′-UCACUCUUGUCCACAGU-X- 3′-(SEQ ID NO. 171)-5′- AS171 UGACACCUGUUCUCACU-3′ X-5′-(SEQ ID NO. 171)-3′ 172/ MDM2 RNA (h) 3′-ACUCACUCUUGUCCACAGU-X- 3′-(SEQ ID NO. 172)-5′- AS172 UGACACCUGUUCUCACUCA-3′ X-5′-(SEQ ID NO. 172)-3′ 173/ MDM2 RNA (h) 3′-ACACUCACUCUUGUCCACAGU-X- 3′-(SEQ ID NO. 173)-5′- AS173 UGACACCUGUUCUCACUCACA-3′ X-5′-(SEQ ID NO. 173)-3′ 174/ MDM2 RNA (m) 3′-GGACUUCCACCCUCACUAG-X- 3′-(SEQ ID NO. 174)-5′- AS174 GAUCACUCCCACCUUCAGG-3′ X-5′-(SEQ ID NO. 174)-3′ 175/ VEGF RNA (h) 3′-CACCCAAGACAGCAGAAAG-X- 3′-(SEQ ID NO. 175)-5′- AS175 GAAAGACGACAGAACCCAC-3′ X-5′-(SEQ ID NO. 175)-3′ 176/ miR-21 RNA (h) 3′-CGAAUAGUCUGACUACAAC-X- 3′-(SEQ ID NO. 176)-5′- AS176 CAACAUCAGUCUGAUAAGC-3′ X-5′-(SEQ ID NO. 176)-3′ 177/ miR-21 RNA (h) 3′-CG 

 AUA 

 UCU 

 AC 3′-(SEQ ID NO. 177)-5′- AS177

 AC 

 AC-X-CA 

 CA 

X-5′-(SEQ ID NO. 177)-3′ CA 

 UCU 

 AUA 

 GC-3′ 178/ miR-21 DNA (h) 3′-CGAATAGTCTGACTACAAC-X- 3′-(SEQ ID NO. 178)-5′- AS178 CAACATCAGTCTGATAAGC-3′ X-5′-(SEQ ID NO. 178)-3′ 179/ miR-21 DNA (h) 3′-CG 

 ATA 

 TCT 

 AC 3′-(SEQ ID NO. 179)-5′- AS179

 AC 

 AC-X-CA 

 CA 

  X-5′-(SEQ ID NO. 179)-3′ CA 

 TCT 

 ATA 

 GC-3′ X = glycerol linker; X1 = 1,2,4-Butanetriol linker; X3 = 2-Hydroxymethyl-1,3-propanediol linker; X5 = Bis-1,5-O-(3′thymidyl)-1,3,5-Pentanetriol Linker; Y = 1,3-Propanediol linker; Z = 1,3,5-Pentanetriol linker; M = cis,cis-1,3,5-Cyclohexanetriol linker; L = cis,trans-1,3,5-Cyclohexanetriol linker; A, U, C, G = 2′-OMe;

,

,

,

,

, = mismatched basepair; o = phosphodiester internucleotide linkage; h = human; m = mouse; Except where indicated, all molecules in Table 3 contain phosphorothioate internucleotide linkages.

In this aspect of the invention, the composition lacks immune stimulatory activity of certain oligonucleotide compositions. It is known that certain oligonucleotide-based compositions can possess immune stimulatory motifs. This immune stimulatory activity requires the oligonucleotides to be non-linked or linked at their 3′ ends. Thus, it is contemplated that as a result of the oligonucleotide-based compositions according to the invention utilizing a linkage at the 5′ ends, as set forth in Formulas I, II, III or IV, that any inherent immune stimulatory activity is suppressed, as compared to the immune stimulatory activity that would be present in non-linked or oligonucleotide-based compositions linked at their 3′ ends or in a 2′-5′ fashion.

The inventors have surprisingly discovered that the structure of the oligonucleotide-based compound according to the invention provides an optimal compound for binding by enzymes and other proteins that are involved in RNaseH-mediated and/or RNAi-mediated inhibition of gene expression. Thus, in a further embodiment of this aspect of the invention, the oligonucleotide-based compounds according to the invention can be selectively bound by RNaseH, Dicer, Argonaut, RISC or other proteins that are involved in RNAi-mediated inhibition of gene expression. This selective binding provides optimal oligonucleotide-based compounds for utilizing RNaseH-mediated and/or RNAi-mediated inhibition of miRNA activity in vitro and in vivo.

In a second aspect, the invention provides pharmaceutical formulations comprising an oligonucleotide-based compound according to the invention and a physiologically acceptable carrier.

In a third aspect, the invention provides a method for inhibiting miRNA activity, the method comprising contacting a cell with a synthetic oligonucleotide-based compound according to the first aspect of the invention.

In a fourth aspect, the invention provides a method for inhibiting miRNA activity in a mammal, the method comprising administering to the mammal a synthetic oligonucleotide-based compound according to the first aspect of the invention. In a further embodiment of this aspect of the invention, it is contemplated that the synthetic oligonucleotide-based compounds according to the first aspect of the invention can inhibit the activity of certain miRNA related to cellular proliferation.

In a fifth aspect, the invention provides a method of inhibiting a response mediated by a microRNA (miRNA) in a mammal though administration of a synthetic oligonucleotide-based compound according to the first aspect of the invention wherein the oligonucleotides are complementary to one or more miRNA sequence. In certain preferred embodiments, the miRNA is miR-21. In certain preferred embodiments, the response is oncogenesis. In certain embodiments, the response is resistance to apoptosis.

In a sixth aspect, the invention provides a method of inhibiting a response mediated by a miRNA in a mammal through administration of a synthetic oligonucleotide-based compound according to the first aspect of the invention wherein the oligonucleotides are complementary to one or more miRNA sequence in combination with an antagonist of RISC activity. In certain preferred embodiments, the miRNA is miR-21. In certain preferred embodiments, the response is oncogenesis. In certain embodiments, the response is resistance to aptoptosis.

In a seventh aspect, the invention provides methods for inhibiting miRNA activity in a mammal, such methods comprising administering to the mammal an oligonucleotide-based compound according to the invention. In some embodiments, the mammal is a human. In preferred embodiments, the oligonucleotide-based compound according to the invention is administered to a mammal in need of inhibiting its miRNA-mediated response.

In a eighth aspect, the invention provides methods for therapeutically treating a patient having a disease or disorder, such methods comprising administering to the patient an oligonucleotide-based compound according to the invention in a therapeutically effective amount. In various embodiments, the disease or disorder to be treated is cancer, an autoimmune disorder, infectious disease, airway inflammation, inflammatory disorders, allergy, asthma, or a disease caused by a pathogen. Pathogens include bacteria, parasites, fungi, viruses, viroids, and prions.

In a ninth aspect, the invention provides methods for preventing a disease or disorder, such methods comprising administering to a subject at risk for developing the disease or disorder an oligonucleotide-based compound according to the invention in a pharmaceutically effective amount. A subject is considered at risk for developing a disease or disorder if the subject has been or may be or will be exposed to an etiologic agent of the disease or disorder or is genetically predispositioned to contract the disease or disorder. In various embodiments, the disease or disorder to be prevented is cancer, an autoimmune disorder, airway inflammation, inflammatory disorders, infectious disease, allergy, asthma, or a disease caused by a pathogen. Pathogens include bacteria, parasites, fungi, viruses, viroids, and prions.

In a tenth aspect the invention provides a method of preventing or treating a disorder, such methods comprises isolating cells capable of producing cytokines or chemokines including, but not limited to, immune cells, T-regulatory cells, B-cells, PBMCs, pDCs, and lymphoid cells; culturing such cells under standard cell culture conditions, treating such cells ex vivo with an oligonucleotide-based compound according to the first aspect of the invention such that the isolated cells produce or secrete decreased levels of cytokines or chemokines, and administering or re-administering the treated cells to a patient in need of therapy to inhibit cytokines and/or chemokine for the prevention and/or treatment of disease. This aspect of the invention would be in accordance with standard adoptive cellular immunotherapy techniques to produce activated immune cells.

In some embodiments of this aspect of the invention, the cells capable of producing cytokines or chemokines may be isolated from subjects with or without a disease or disorder. Such isolation may include identification and selection and could be performed using standard cell isolation procedures, including those set forth in the specific examples below. Such isolated cells would be cultured according to standard cell culturing procedures and using standard cell culture conditions, which may include the culturing procedures and conditions set forth in the specific examples below. In a further aspect of this embodiment of the invention, the isolated cells would be cultured in the presence of at least one oligonucleotide-based compound according to the invention, in an amount and for a time period sufficient to suppress or inhibit the production and/or secretion of cytokines and/or chemokines as compared to the isolated cells cultured in the absence of such one or more oligonucleotide-based compound according to the invention. Such time may be from minutes, to hours, to days. Such isolated and treated cells may find use following re-administration to the donor or administration to a second patient, wherein such donor or second patient are in need of suppressed or inhibited production and/or secretion of cytokines and/or chemokines. For example, re-administration to a donor or administration to a second patient having cancer, an autoimmune disorder, airway inflammation, inflammatory disorders, infectious disease, allergy, asthma, or a disease caused by a pathogen. Such re-administration or administration may be accomplished using various modes, including catheter or injection administration or any other effective route. This aspect of the invention may also find use in patients who may have a limited or incomplete ability to mount an immune response or are immune compromised (e.g. patient infected with HIV and bone marrow transplant patients).

In an eleventh aspect, the invention provides a composition comprising a compound according to the first aspect of the invention and one or more vaccines, antigens, antibodies, cytotoxic agents, chemotherapeutic agents (both traditional chemotherapy and modern targeted therapies), kinase inhibitors, allergens, antibiotics, agonist, antagonist, antisense oligonucleotides, ribozymes, RNAi molecules, siRNA molecules, miRNA molecules, aptamers, proteins, gene therapy vectors, DNA vaccines, adjuvants, co-stimulatory molecules or combinations thereof.

In any of the methods according to the invention, the oligonucleotide-based compound according to the invention can variously act by producing direct miRNA activity effects alone and/or in combination with any other agent useful for treating or preventing the disease or condition that does not diminish the miRNA activity inhibiting effect of the oligonucleotide-based compound according to the invention. In any of the methods according to the invention, the agent(s) useful for treating or preventing the disease or condition includes, but is not limited to, vaccines, antigens, antibodies, preferably monoclonal antibodies, cytotoxic agents, kinase inhibitors, allergens, antibiotics, siRNA molecules, antisense oligonucleotides, TLR antagonist (e.g. antagonists of TLR3 and/or TLR7 and/or antagonists of TLR8 and/or antagonists of TLR9), chemotherapeutic agents (both traditional chemotherapy and modern targeted therapies), targeted therapeutic agents, activated cells, peptides, proteins, gene therapy vectors, peptide vaccines, protein vaccines, DNA vaccines, adjuvants, and co-stimulatory molecules (e.g. cytokines, chemokines, protein ligands, trans-activating factors, peptides or peptides comprising modified amino acids), or combinations thereof. For example, in the treatment of cancer, it is contemplated that the oligonucleotide-based compound according to the invention may be administered in combination with one or more chemotherapeutic compound, targeted therapeutic agent and/or monoclonal antibody. Alternatively, the agent can include DNA vectors encoding for antigen or allergen. Alternatively, the oligonucleotide-based compound according to the invention can be administered in combination with other compounds (for example lipids or liposomes) to enhance the specificity or magnitude of the gene expression modulation of the oligonucleotide-based compound according to the invention.

In any of the methods according to the invention, administration of oligonucleotide-based compounds according to the invention, alone or in combination with any other agent, can be by any suitable route, including, without limitation, parenteral, mucosal delivery, oral, sublingual, transdermal, topical, inhalation, intranasal, aerosol, intraocular, intratracheal, intrarectal, vaginal, by gene gun, dermal patch or in eye drop or mouthwash form. Administration of the therapeutic compositions of oligonucleotide-based compounds according to the invention can be carried out using known procedures using an effective amount and for periods of time effective to reduce symptoms or surrogate markers of the disease. For example, an effective amount of an oligonucleotide-based compound according to the invention for treating a disease and/or disorder could be that amount necessary to alleviate or reduce the symptoms, or delay or ameliorate a tumor, cancer, or bacterial, viral or fungal infection. In the context of administering a composition that modulates gene expression, an effective amount of an oligonucleotide-based compound according to the invention is an amount sufficient to achieve the desired modulation as compared to the gene expression in the absence of the oligonucleotide-based compound according to the invention. The effective amount for any particular application can vary depending on such factors as the disease or condition being treated, the particular oligonucleotide being administered, the size of the subject, or the severity of the disease or condition. One of ordinary skill in the art can empirically determine the effective amount of a particular oligonucleotide without necessitating undue experimentation.

When administered systemically, the therapeutic composition is preferably administered at a sufficient dosage to attain a blood level of oligonucleotide-based compound according to the invention from about 0.0001 micromolar to about 10 micromolar. For localized administration, much lower concentrations than this may be effective, and much higher concentrations may be tolerated. Preferably, a total dosage of oligonucleotide-based compound according to the invention ranges from about 0.001 mg per patient per day to about 200 mg per kg body weight per day. In certain embodiments, the total dosage may be 0.08, 0.16, 0.32, 0.48, 0.32, 0.64, 1, 10 or 30 mg/kg body weight administered daily, twice weekly or weekly. It may be desirable to administer simultaneously, or sequentially a therapeutically effective amount of one or more of the therapeutic compositions of the invention to an individual as a single treatment episode.

The methods according to this aspect of the invention are useful for model studies of miRNA activity. The methods are also useful for the prophylactic or therapeutic treatment of human or animal disease. For example, the methods are useful for pediatric and veterinary inhibition of gene expression applications.

The examples below are intended to further illustrate certain preferred embodiments of the invention, and are not intended to limit the scope of the invention.

Example 1 Preparation of Oligonucleotide-Based Compounds

The oligonucleotide-based compounds of the invention were chemically synthesized using phosphoramidite chemistry on automated DNA/RNA synthesizer. TAC protected (Except U) 2′-O-TBDMS RNA monomers, A, G, C and U, were purchased from Sigma-Aldrich. 7-deaza-G, inosine and loxoribine monomers were purchased from ChemGenes Corporation. 0.25M 5-ethylthio-1H-tetrazole, PAC-anhydride Cap A and Cap B were purchased from Glen Research. 3% trichloroacetic acid (TCA) in dichloromethane (DCM) and 5% 3H-1,2-Benzodithiole-3-one-1,1-dioxide (Beaucage reagent) were made in house.

Oligonucleotide-based compounds of the invention were synthesized at 1-2 μM scale using a standard RNA synthesis protocol.

Cleavage and Base Deprotection

Oligonucleotide-based compounds of the invention were cleaved from solid support and the solution was further heated at 65° C. to removing protecting groups of exo cyclic-amines. The resulting solution was dried completely in a SpeedVac.

IE HPLC Purification

Oligonucleotide-based compounds of the invention were purified by ion exchange HPLC.

Column: Dionex DNAPac 100 column (22×250)

Column Heater ChromTech TL-105 HPLC column heater, temperature is set to 80° C.

Buffer A: 20 mM Tris-HCl, pH 7.0, 20% acetinitrile

Buffer B: 3.0 M NaCl, 20 mM Tris-HCl, pH 7.0, 20% acetonitrile

Flow rate: 10 ml/min

Gradient:

-   -   0-2 min: 0% B     -   2-11 min: 0% B to 35% B     -   11-41 min: 35% B to 90% B     -   41-45 min: 100% B

Crude solution of oligonucleotide-based compounds of the invention was injected into HPLC. Above gradient is performed and the fractions were collected. All fractions containing more than 90% desired product were mixed, and then the solution was concentrated to almost dry by RotoVap. RNAse-free water was added to make final volume of 10 ml.

C-18 Reversed Phase Desalting

CC-18 Sep-Pak cartridge purchased from Waters was first conditioned with 10 ml of acetonitrile followed by 10 ml of 0.5 M sodium acetate. 10 ml of the solution of oligonucleotide-based compounds of the invention was loaded. 15 ml of water was then used to wash out the salt. The oligonucleotide-based compounds of the invention was eluted out by 1 ml of 50% acetonitrile in water.

The solution is placed in SpeedVac for 30 minutes. The remaining solution was filter through a 0.2 micro filter and then was lyophilized to dryness. The solid was then re-dissolved in water to make the desired concentration.

The final solution was stored below 0° C.

Capillary Electrophoresis

Oligonucleotide-based compounds of the invention were analyzed by capillary electrophoresis according to the following conditions.

Instrument: Beckman 5010

Capillary: 62 cm ssDNA capillary

Sample preparation: 0.2 OD of oligonucleotide-based composition according to the invention was dissolved in 200 ul of RNAse-free water.

Injection: electro-kinetic injection at 5 KV for 5 seconds.

Running condition: 14 KV for 50 minutes at 30° C.

Ion Exchange HPLC Analysis

Oligonucleotide-based compounds of the invention were analyzed by ion exchange HPLC according to the following conditions

Column: Dionex DNAPac guard column (22×250)

Column Heater ChromTech TL-105 HPLC column heater, temperature is set to 80° C.

Buffer A: 100 mM Tris-HCl, pH 8.0, 20% acetinitrile

Buffer B: 2.0 M LiCl, 100 mM Tris-HCl, pH 8.0, 20% acetonitrile

Flow rate: 2 ml/min

Gradient:

-   -   0-2 min: 0% B     -   2-10 min: 0% B to 100% B     -   10-15 min: 100% B

PAGE Analysis

0.3 OD of oligonucleotide-based compounds of the invention was loaded on 20% polyacrylamide gel and was running at constant power of 4 watts for approximately 5 hours. The gel was viewed under short wavelength UV light.

Example 2 Human PBMC Isolation

Peripheral blood mononuclear cells (PBMCs) from freshly drawn healthy volunteer blood (CBR Laboratories, Boston, Mass.) were isolated by Ficoll density gradient centrifugation method (Histopaque-1077, Sigma).

Human pDC Isolation

Human plasmacytoid dendritic cells (pDCs) were isolated from freshly obtained healthy human volunteer's blood PBMCs by positive selection using the BDCA4 cell isolation kits (Miltenyi Biotec) according to the manufacturer's instructions.

Treatment of PBMCs and pDCs

Human PBMCs were plated in 48-well plates using 5×10⁶ cells/ml. Human pDCs were plated in 96-well dishes using 1×10⁶ cells/ml. The exemplary oligonucleotide-based compounds of the invention, dissolved in DPBS (pH 7.4; Mediatech), were added to the cell cultures at doses of 0, 0.01, 1.0 or 10.0 μg/ml. The cells were then incubated at 37° C. for 24 hours and subsequently stimulated with 10 μg/ml TLR9 agonist for 24 h. After treatment and stimulation, the supernatants were collected for luminex multiplex or ELISA assays. In certain experiments, the levels of IFN-α, IL-6, and/or IL-12 were measured by sandwich ELISA. The required reagents, including cytokine antibodies and standards, were purchased from PharMingen.

Human B Cell Assay for TLR9 Antisense Activity

Human B cells were isolated from PBMCs by positive selection using the CD19 Cell Isolation Kit (Miltenyi Biotec, Auburn, Calif.) according to the manufacturer's instructions.

The culture medium used for the assay consisted of RPMI 1640 medium supplemented with 1.5 mM glutamine, 1 mM sodium pyruvate, 0.1 mM non-essential amino acids, 50 μM 2-mercaptoethanol, 100 IU/ml penicillin-streptomycin mix and 10% heat-inactivated fetal bovine serum.

A total of 0.5×10⁶ B cells per ml (i.e. 1×10⁵/200 μl/well) were incubated in 96 well flat bottom plates with 50 μg/ml of exemplary oligonucleotide-based compounds of the invention for 24 hours. After 24 hours, cells were stimulated with 10 μg/ml TLR9 agonist for 24 h. Following treatment and stimulation, cell extracts were prepared and analyzed for the amount of TLR9 mRNA.

HEK293 Cell Culture Assays for TLR9 or TLR7 Antisense Activity

HEK293 cells stably expressing mouse TLR9 or TLR7 (Invivogen, San Diego, Calif.), were plated in 48-well plates in 250 μL/well DMEM supplemented with 10% heat-inactivated FBS in a 5% CO2 incubator. At 80% confluence, cultures were transiently transfected with 400 ng/mL of the secreted form of human embryonic alkaline phosphatase (SEAP) reporter plasmid (pNifty2-Seap) (Invivogen) in the presence of 4 μL/mL of lipofectamine (Invitrogen, Carlsbad, Calif.) in culture medium. Plasmid DNA and lipofectamine were diluted separately in serum-free medium and incubated at room temperature for 5 min. After incubation, the diluted DNA and lipofectamine were mixed and the mixtures were incubated further at room temperature for 20 min. Aliquots of 25 μL of the DNA/lipofectamine mixture containing 100 ng of plasmid DNA and 1 μL of lipofectamine were added to each well of the cell culture plate, and the cells were transfected for 6 h. After transfection, medium was replaced with fresh culture medium (no antibiotics) and 0, 0.01, 1 or 10 μg/ml of TLR9 or TLR7 specific oligonucleotide-based compounds of the invention were added to the wells, and incubation continued for 24 h. Following antisense treatment, cells were then stimulated with the 10 μg/ml TLR9 or TLR7 agonist for 24 h.

At the end of the treatment and stimulation, 20 μL of culture supernatant was taken from each well and assayed for SEAP assay by the Quanti Blue method according to the manufacturer's protocol (Invivogen). The data are shown as fold increase in NF-κB activity over PBS control.

HEK293 Cell Culture Assays for TLR7, TLR8 or Other Specific RNA Target Antisense Activity

For determining the activity of antisense oligonucleotides according to the invention to inhibit TLR7 or TLR8 or any other specific RNA target, the following procedure would be followed: HEK293 cells stably expressing mouse TLR7 or TLR8 or another specific RNA target (Invivogen, San Diego, Calif.), would be plated in 48-well plates in 250 μL/well DMEM supplemented with 10% heat-inactivated FBS in a 5% CO2 incubator. At 80% confluence, cultures would be transiently transfected with 400 ng/mL of the secreted form of human embryonic alkaline phosphatase (SEAP) reporter plasmid (pNifty2-Seap) (Invivogen) in the presence of 4 μL/mL of lipofectamine (Invitrogen, Carlsbad, Calif.) in culture medium. Plasmid DNA and lipofectamine would be diluted separately in serum-free medium and incubated at room temperature for 5 min. After incubation, the diluted DNA and lipofectamine would be mixed and the mixtures would be incubated further at room temperature for 20 min. Aliquots of 25 μL of the DNA/lipofectamine mixture containing 100 ng of plasmid DNA and 1 μL of lipofectamine would be added to each well of the cell culture plate, and the cells would be transfected for 6 h. After transfection, medium would be replaced with fresh culture medium (no antibiotics) and 0, 0.01, 1 or 10 μg/ml of specific antisense oligonucleotides according to the invention would be added to the wells, and incubation continued for 24 h. Following antisense treatment, the cells would be stimulated with the target's agonist for up to 24 h.

At the end of the treatment and stimulation, 20 μL of culture supernatant would be taken from each well and assayed for SEAP assay by the Quanti Blue method according to the manufacturer's protocol (Invivogen). The data would be shown as fold increase in NF-κB activity over PBS control.

Murine J774 Cell Assay for TLR9 Antisense Activity

Murine J774 macrophage cells (American Type Culture Collection, Rockville, Md.) were cultured in Dulbecco's modified Eagle's medium supplemented with 10% (v/v) fetal bovine serum (FBS) and antibiotics (100 IU/ml penicillin G/100 μg/ml streptomycin). J774 cells were plated at a density of 5×10⁶ cells/well in six-well plates. For dose dependent experiments, the J774 cells were then treated with 0, 1, 10, 50 or 100 μg/ml of TLR9 specific oligonucleotide-based compounds of the invention and incubation continued for 24 h. For experiments determining the effects on mRNA, the J774 cells were then treated with 0, 1 or 3 μg/ml of TLR9 specific oligonucleotide-based compounds of the invention or control oligonucleotides and incubation continued for 48 h. For experiments determining the effects on protein, the J774 cells were then treated with 0, or 50 μg/ml of TLR9 specific oligonucleotide-based compounds of the invention or control oligonucleotides and incubation continued for 48 h. Following antisense treatment, cellular extracts were prepared and analyzed for the amount of TLR9 mRNA or TLR9 protein.

HeLa Cell Assay for VEGF Antisense Activity

5×10⁶ HeLa cells (ATCC, Manassas, Va.) were plated in a 12-well culture plate in Dulbecco's Modified Eagle Medium (DMEM, Mediatech, Manassas, Va.) supplemented with 10% fetal bovine serum (FBS, Mediatch, Manassas, Va.). For cell transfection, 5 μl Lipofectamine® 2000 (Invitrogen, Carlsbad, Calif.) and 5 μg antisense oligonucleotides were mixed in 100 μl DMEM without serum and incubated at room temperature for 15 minutes. Cells were washed once with DMEM without serum and 100 μl lipofectamine/oligonucleotide complexes were added to 900 μl DMEM without serum followed by 2 hour incubation at 37° C. with 5% CO₂. A lipofectamine only group served as a control. Medium was then changed to DMEM with 10% FBS and incubated for 24 hours. Following the 24 hour incubation, total RNA was isolated using a QIAGEN RNeasy mini kit (QIAGEN, Valencia, Calif.) according to manufacturer's suggestion. 1 μg RNA was used to reverse transcribe to cDNA using a High Capacity cDNA Reverse Transcription kit (Appliedbiosystems, Carlsbad, Calif.) according to manufacturer's recommendation. For quantitative real-time PCR (qPCR), primers and probes for VEGF (catalog no. Hs00900057 ml) and GAPDH (Hs99999905 ml) were purchased from Applied Biosystems. 50 ng cDNA was used in the qPCR with Taqman® Fast Universal PCR Master Mix (Applied Biosystems) and reactions were run on an Applied Biosystems StepOnePlus™ Real-Time PCR System according to manufacturer's instructions. Data is depicted in FIG. 11D as relative quantity of mRNA to lipofectamine treated cells using the ΔΔCT method, where ΔCT=CT_(VEGF)-CT_(GAPDH) and ΔΔCT=ΔCT_(oligonucleotide)-ΔCT_(lipofectamine). Each bar represents 2-3 separate experiments.

C57BL/6 Mouse Splenocyte Cell Assay for TLR9 Antisense Activity

Spleen cells from 4- to 8-week old C57BL/6 mice were cultured in RPMI complete medium. Mouse spleen cells were plated in 24-well dishes using 5×10⁶ cells/ml, treated with TLR9 specific oligonucleotide-based compounds of the invention dissolved in TE buffer (10 mM Tris-HCl, pH 7.5, 1 mM EDTA), and incubated at 37° C. for 24 hrs. Following antisense treatment, cells were then stimulated with 10 μg/ml TLR9 agonist for 24 hrs. After treatment and stimulation, the supernatants were collected and the secretion of IL-12 and IL-6 in cell culture supernatants was measured by sandwich ELISA.

Example 3 In Vivo Activity of Oligonucleotide-Based Compositions

To assess the in vivo activity of antisense oligonucleotides according to the invention, Female C57BL/6 mice of 5-6 weeks age (N=3/group) were injected with exemplary oligonucleotide-based compositions according to the invention at 0.25, 2, or 5 mg/kg, or PBS, subcutaneously in the left flank. Twenty-four hours after administration of the oligonucleotide-based compositions, mice were injected with 0.25 mg/kg of a TLR agonist subcutaneously in the right flank. Two hours after administration of the TLR agonist, blood was collected and serum IL-12 concentration was determined by ELISA. Data are shown as absolute IL-12 concentrations or as a percentage of IL-12 production.

Duration of In Vivo Activity of Oligonucleotide-Based Compositions

To assess the duration of in vivo activity of antisense oligonucleotides according to the invention, Female C57BL/6 mice of 5-6 weeks age (N=3/group) were injected with exemplary oligonucleotide-based compositions according to the invention at 5 mg/kg, or PBS, subcutaneously in the left flank. Twenty-four hours after administration of the oligonucleotide-based compositions, mice were injected with 0.25 mg/kg of a TLR agonist subcutaneously in the right flank on days 1, 3, 5, 7, 10 or 14. Two hours after each administration of the TLR agonist, blood was collected and serum IL-12 concentration was determined by ELISA. Data are shown as absolute IL-12 concentrations or as a percentage of IL-12 production.

Example 4 Selective Binding and Cleavage of Oligonucleotide-Based Compounds by Antisense-Associated Proteins and Enzymes

To assess the specificity for antisense-associated proteins and enzymes to bind and cleave oligonucleotide-based compounds according to the invention or control oligonucleotides, were treated as follows: The 5′-end [γ-32P] labeled target mRNA (e.g. SED ID NO. 21; 10 nM human/mouse TLR7) and complementary RNA or DNA (10 nM; human/mouse TLR7) in 30 ml of Buffer (10× buffer, Invitrogen) were heated at 85° C. for 5 min, and then cooled down to room temperature for 20 min to allow annealing of the two strands. The human dicer enzyme (0.025 U, Invitrogen) was added to reaction solution, and then incubated at 37° C. for 1 hr. 1 ml of stop solution (Invitrogen) and 10 ml of gel loading dye were added to sample solution and mixed well. The sample was frozen immediately at −80° C. RNA digestion products were analyzed on 16% denaturing PAGE and the gel was exposed to x-ray film and the autoradiogram was developed. Results are shown in FIG. 16.

Example 5 Knockdown of microRNA, miR-21

To assess the ability of GSOs targeted to miRNA to effectively reduce the amount of miRNA present for the selected miRNA, approximately 1.35×10⁶ cells of the human colorectal carcinoma cell line HCT-116 were cultured in each well of 6-well culture plates in 1.8 ml of DMEM supplemented with 10% heat-inactivated FBS in a 5% CO2 incubator. Once the cells reached 80% confluence, cultures were transiently transfected with GSOs at a final concentration of 2 mg/ml or 10 mg/ml in the presence of Lipofectamine (Invitrogen, Carlsbad, Calif.) at a final concentration of 1 ml/ml in culture medium. After a 48 hour incubation, RNA was extracted from cells according to the protocol given in the miRNeasy Mini Kit (Qiagen, Valencia, Calif.). RNA was quantified by an ultraviolet spectrophotometer at a wavelength of 260 nm. Reverse transcription was carried out for each sample using components of the TaqMan MicroRNA Reverse Transcription Kit in conjunction with the RT primer provided with the TaqMan MicroRNA Assay (Applied Biosystems, Carlsbad, Calif.) for miR-21 and the endogenous control RNU44. Real-time PCR was carried out on the StepOnePlus Real-Time PCR System (Applied Biosystems, Carlsbad, Calif.) and the reactions were set up using the TaqMan® Fast Universal PCR Master Mix (2×), No AmpErase® UNG along with the TaqMan MicroRNA Assay for miR-21 and RNU44 according to the TaqMan Small RNA Assays protocol provided by Applied Biosystems. Data were analyzed using StepOnePlus software and the efficacy of miR-21 antisense oligonucleotides was determined in relation to mismatch oligonucleotides corresponding to each antisense compound. Results are shown in FIG. 17.

EQUIVALENTS

Those skilled in the art will recognize, or be able to ascertain, using no more than routine experimentation, numerous equivalents to the specific substances and procedures described herein. For example, antisense oligonucleotides that overlap with the oligonucleotides may be used. Such equivalents are considered to be within the scope of this invention, and are covered by the following claims. 

What is claimed is:
 1. A method for therapeutically treating a mammal having a disease or disorder mediated by a miRNA, the method comprising administering to the mammal a synthetic oligonucleotide-based compound comprising two single stranded oligonucleotides that are complementary to a miRNA sequence, wherein the oligonucleotides are linked at their 5′-ends such that the oligonucleotide-based compound has two accessible 3′-ends, and the oligonucleotides specifically hybridize to and inhibit the activity of the miRNA sequence.
 2. A method for preventing a disease or disorder mediated by one or more miRNA in a mammal at risk for developing the disease or disorder, the method comprising administering to the mammal a synthetic oligonucleotide-based compound comprising two single stranded oligonucleotides that are complementary to a miRNA sequence, wherein the oligonucleotides are linked at their 5′-ends such that the oligonucleotide-based compound has two accessible 3′-ends, and the oligonucleotides specifically hybridize to and inhibit the activity of the miRNA sequence.
 3. The method according to claim 1 or 2 wherein the disease or disorder is cancer.
 4. The method according to claim 1 or 2, wherein the mammal is a human.
 5. The method according to claim 1 or 2 wherein the miRNA sequence is miR-21.
 6. The method according to claim 1 or 2, wherein the oligonucleotides are independently 15 to 22 nucleotides in length.
 7. The method according to claim 1 or 2, wherein the oligonucleotides comprise one or more ribonucleotides, deoxyribonucleotides, locked nucleic acids, arabino sugar nucleotides or a combination thereof.
 8. The method according to claim 1 or 2, wherein at least one of the oligonucleotides is modified.
 9. The method according to claim 8, wherein the modified oligonucleotide has at least one internucleotide linkage selected from the group consisting of alkylphosphonate, phosphorothioate, phosphorodithioate, methylphosphonate, and non-nucleotide linker.
 10. The method according to claim 8, wherein the modified oligonucleotide comprises at least one 2′-O-substituted nucleotide.
 11. The method according to claim 10, wherein the 2′-O-substitution is selected from 2′-β-methyl, 2′-O-methoxy, 2′-O-ethoxy, 2′-O-methoxyethyl, 2′-O-alkyl, 2′-O-aryl, and 2′-O-allyl.
 12. The method according to claim 1 or 2, further comprising administering one or more vaccines, antigens, antibodies, cytotoxic agents, allergens, antibiotics, antisense oligonucleotides, TLR agonist, TLR antagonist, siRNA molecules, miRNA molecules, antisense oligonucleotides, aptamers, proteins, peptides, gene therapy vectors, adjuvants, kinase inhibitors, chemotherapeutic agents, targeted therapeutic agents, activated cells, co-stimulatory molecules or combinations thereof.
 13. The method according to claim 12, wherein the vaccine is a DNA vaccine, peptide vaccine, or protein vaccine.
 14. A method for inhibiting in vivo miRNA activity, the method comprising administering to a mammal an oligonucleotide-based compound comprising two single-stranded oligonucleotides that are complementary to a miRNA sequence, wherein the oligonucleotides are linked at their 5′-ends such that the oligonucleotide-based compound has two accessible 3′-ends, wherein at least one of the oligonucleotides is modified, and the oligonucleotides specifically hybridize to and inhibit the activity of the miRNA sequence.
 15. The method according to claim 14, wherein the oligonucleotides are independently 15 to 22 nucleotides in length.
 16. The method according to claim 14, wherein the oligonucleotides comprise one or more ribonucleotides, deoxyribonucleotides, locked nucleic acids, arabino sugar nucleotides or a combination thereof.
 17. The method according to claim 14, wherein the modified oligonucleotide has at least one internucleotide linkage selected from the group consisting of alkylphosphonate, phosphorothioate, phosphorodithioate, methylphosphonate, and non-nucleotide linker.
 18. The method according to claim 14, wherein the modified oligonucleotide comprises at least one 2′-O-substituted nucleotide.
 19. The method according to claim 18, wherein the 2′-O-substitution is selected from 2′-β-methyl, 2′-O-methoxy, 2′-O-ethoxy, 2′-O-methoxyethyl, 2′-O-alkyl, 2′-O-aryl, and 2′-O-allyl.
 20. The method according to claim 14, further comprising administering one or more vaccines, antigens, antibodies, cytotoxic agents, allergens, antibiotics, antisense oligonucleotides, TLR agonist, TLR antagonist, siRNA molecules, miRNA molecules, antisense oligonucleotides, aptamers, proteins, peptides, gene therapy vectors, adjuvants, kinase inhibitors, chemotherapeutic agents, targeted therapeutic agents, activated cells, co-stimulatory molecules or combinations thereof.
 21. The method according to claim 20, wherein the vaccine is a DNA vaccine, peptide vaccine, or protein vaccine. 